Canonical Allele Identifier: CA381871170

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907604C>A (hg19) ; chr11:g.75196559C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196559C>A , CM000673.2:g.75196559C>A	GRCh38
NC_000011.9:g.74907604C>A , CM000673.1:g.74907604C>A	GRCh37
NC_000011.8:g.74585252C>A	NCBI36
NG_027921.1:g.50573C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1479C>A MANE Select	ENSP00000289575.5:p.Cys493Ter
ENST00000289575.9:c.1479C>A	ENSP00000289575.5:p.Cys493Ter
ENST00000428359.6:c.1413C>A	ENSP00000388912.2:p.Cys471Ter
ENST00000454962.6:c.798C>A	ENSP00000389653.2:p.Cys266Ter
ENST00000525650.5:c.1047C>A	ENSP00000436324.1:p.Cys349Ter
ENST00000528108.1:n.285C>A
ENST00000530012.1:n.306C>A
ENST00000531756.5:n.1026C>A
ENST00000532236.5:c.1131C>A	ENSP00000434112.1:p.Cys377Ter
NM_001145211.2:c.1413C>A	NP_001138683.1:p.Cys471Ter
NM_001145212.2:c.1047C>A	NP_001138684.1:p.Cys349Ter
NM_007256.4:c.1479C>A	NP_009187.1:p.Cys493Ter
XM_017017157.1:c.1485C>A	XP_016872646.1:p.Cys495Ter
NM_001145211.3:c.1413C>A	NP_001138683.1:p.Cys471Ter
NM_001145212.3:c.1047C>A	NP_001138684.1:p.Cys349Ter
NM_007256.5:c.1479C>A MANE Select	NP_009187.1:p.Cys493Ter