Canonical Allele Identifier: CA1983218003

Gene: SLCO2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196547C= , CM000673.2:g.75196547C=	GRCh38
NC_000011.9:g.74907592C= , CM000673.1:g.74907592C=	GRCh37
NC_000011.8:g.74585240C=	NCBI36
NG_027921.1:g.50561C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1467C= MANE Select	ENSP00000289575.5:p.Cys489=
ENST00000289575.9:c.1467C=	ENSP00000289575.5:p.Cys489=
ENST00000428359.6:c.1401C=	ENSP00000388912.2:p.Cys467=
ENST00000454962.6:c.786C=	ENSP00000389653.2:p.Cys262=
ENST00000525650.5:c.1035C=	ENSP00000436324.1:p.Cys345=
ENST00000528108.1:n.273C=
ENST00000530012.1:n.294C=
ENST00000531756.5:n.1014C=
ENST00000532236.5:c.1119C=	ENSP00000434112.1:p.Cys373=
NM_001145211.2:c.1401C=	NP_001138683.1:p.Cys467=
NM_001145212.2:c.1035C=	NP_001138684.1:p.Cys345=
NM_007256.4:c.1467C=	NP_009187.1:p.Cys489=
XM_017017157.1:c.1473C=	XP_016872646.1:p.Cys491=
NM_001145211.3:c.1401C=	NP_001138683.1:p.Cys467=
NM_001145212.3:c.1035C=	NP_001138684.1:p.Cys345=
NM_007256.5:c.1467C= MANE Select	NP_009187.1:p.Cys489=