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IKMB: Blood Group DB

OK > BSG

Genetic changes
Quick Filter:
nt change aa change Location hg19 hg38 rsNum
c.176G>T p.Gly59Val Exon 2 chr19:579608 chr19:579608 rs1023817527
c.178G>A p.Val60Met Exon 2 chr19:579610 chr19:579610 rs2229662
c.274G>A p.Glu92Lys Exon 3 chr19:580428 chr19:580428 rs104894669

basigin
Chromosome:chr19
Strand:+
Genomic ref.:NG_007468.1
Transcript ref.:NM_198589.2
Protein ref.: NP_001309172.1 NP_001719.2 NP_940991.1 NP_940992.1 NP_940993.1 XP_016882662.1
Entrez GeneID:682
Uniprot ID:P35613
Further links:GTEx Portal, gnomAD
hg19:
ExonsStartEndCDS StartCDS End
8 572595 583493 572634 582577
hg38:
ExonsStartEndCDS StartCDS End
8 572595 583493 572634 582577
Exon hg19 start hg19 end hg38 start hg38 end
1 572595 572701 572595 572701
2 579499 579656 579499 579656
3 580378 580461 580378 580461
4 580645 580782 580645 580782
5 581314 581591 581314 581591
6 582305 582330 582305 582330
7 582513 582582 582513 582582
8 582749 583493 582749 583493