Canonical Allele Identifier: CA1983218002

Gene: SLCO2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196546G= , CM000673.2:g.75196546G=	GRCh38
NC_000011.9:g.74907591G= , CM000673.1:g.74907591G=	GRCh37
NC_000011.8:g.74585239G=	NCBI36
NG_027921.1:g.50560G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1466G= MANE Select	ENSP00000289575.5:p.Cys489=
ENST00000289575.9:c.1466G=	ENSP00000289575.5:p.Cys489=
ENST00000428359.6:c.1400G=	ENSP00000388912.2:p.Cys467=
ENST00000454962.6:c.785G=	ENSP00000389653.2:p.Cys262=
ENST00000525650.5:c.1034G=	ENSP00000436324.1:p.Cys345=
ENST00000528108.1:n.272G=
ENST00000530012.1:n.293G=
ENST00000531756.5:n.1013G=
ENST00000532236.5:c.1118G=	ENSP00000434112.1:p.Cys373=
NM_001145211.2:c.1400G=	NP_001138683.1:p.Cys467=
NM_001145212.2:c.1034G=	NP_001138684.1:p.Cys345=
NM_007256.4:c.1466G=	NP_009187.1:p.Cys489=
XM_017017157.1:c.1472G=	XP_016872646.1:p.Cys491=
NM_001145211.3:c.1400G=	NP_001138683.1:p.Cys467=
NM_001145212.3:c.1034G=	NP_001138684.1:p.Cys345=
NM_007256.5:c.1466G= MANE Select	NP_009187.1:p.Cys489=