Canonical Allele Identifier: CA6188403

Gene: SLCO2B1

Linked Data

• dbSNP Id: rs752102813
• ExAC: 11:74907599 G / A
• gnomAD v2: 11-74907599-G-A
• gnomAD v3: 11-75196554-G-A
• gnomAD v4: 11-75196554-G-A
• MyVariant Identifiers: chr11:g.74907599G>A (hg19) ; chr11:g.75196554G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196554G>A , CM000673.2:g.75196554G>A	GRCh38
NC_000011.9:g.74907599G>A , CM000673.1:g.74907599G>A	GRCh37
NC_000011.8:g.74585247G>A	NCBI36
NG_027921.1:g.50568G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1474G>A MANE Select	ENSP00000289575.5:p.Ala492Thr
ENST00000289575.9:c.1474G>A	ENSP00000289575.5:p.Ala492Thr
ENST00000428359.6:c.1408G>A	ENSP00000388912.2:p.Ala470Thr
ENST00000454962.6:c.793G>A	ENSP00000389653.2:p.Ala265Thr
ENST00000525650.5:c.1042G>A	ENSP00000436324.1:p.Ala348Thr
ENST00000528108.1:n.280G>A
ENST00000530012.1:n.301G>A
ENST00000531756.5:n.1021G>A
ENST00000532236.5:c.1126G>A	ENSP00000434112.1:p.Ala376Thr
NM_001145211.2:c.1408G>A	NP_001138683.1:p.Ala470Thr
NM_001145212.2:c.1042G>A	NP_001138684.1:p.Ala348Thr
NM_007256.4:c.1474G>A	NP_009187.1:p.Ala492Thr
XM_017017157.1:c.1480G>A	XP_016872646.1:p.Ala494Thr
NM_001145211.3:c.1408G>A	NP_001138683.1:p.Ala470Thr
NM_001145212.3:c.1042G>A	NP_001138684.1:p.Ala348Thr
NM_007256.5:c.1474G>A MANE Select	NP_009187.1:p.Ala492Thr