Canonical Allele Identifier: CA381871164

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907602T>A (hg19) ; chr11:g.75196557T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196557T>A , CM000673.2:g.75196557T>A	GRCh38
NC_000011.9:g.74907602T>A , CM000673.1:g.74907602T>A	GRCh37
NC_000011.8:g.74585250T>A	NCBI36
NG_027921.1:g.50571T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1477T>A MANE Select	ENSP00000289575.5:p.Cys493Ser
ENST00000289575.9:c.1477T>A	ENSP00000289575.5:p.Cys493Ser
ENST00000428359.6:c.1411T>A	ENSP00000388912.2:p.Cys471Ser
ENST00000454962.6:c.796T>A	ENSP00000389653.2:p.Cys266Ser
ENST00000525650.5:c.1045T>A	ENSP00000436324.1:p.Cys349Ser
ENST00000528108.1:n.283T>A
ENST00000530012.1:n.304T>A
ENST00000531756.5:n.1024T>A
ENST00000532236.5:c.1129T>A	ENSP00000434112.1:p.Cys377Ser
NM_001145211.2:c.1411T>A	NP_001138683.1:p.Cys471Ser
NM_001145212.2:c.1045T>A	NP_001138684.1:p.Cys349Ser
NM_007256.4:c.1477T>A	NP_009187.1:p.Cys493Ser
XM_017017157.1:c.1483T>A	XP_016872646.1:p.Cys495Ser
NM_001145211.3:c.1411T>A	NP_001138683.1:p.Cys471Ser
NM_001145212.3:c.1045T>A	NP_001138684.1:p.Cys349Ser
NM_007256.5:c.1477T>A MANE Select	NP_009187.1:p.Cys493Ser