Canonical Allele Identifier: CA1983218005

Gene: SLCO2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196550G= , CM000673.2:g.75196550G=	GRCh38
NC_000011.9:g.74907595G= , CM000673.1:g.74907595G=	GRCh37
NC_000011.8:g.74585243G=	NCBI36
NG_027921.1:g.50564G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1470G= MANE Select	ENSP00000289575.5:p.Met490=
ENST00000289575.9:c.1470G=	ENSP00000289575.5:p.Met490=
ENST00000428359.6:c.1404G=	ENSP00000388912.2:p.Met468=
ENST00000454962.6:c.789G=	ENSP00000389653.2:p.Met263=
ENST00000525650.5:c.1038G=	ENSP00000436324.1:p.Met346=
ENST00000528108.1:n.276G=
ENST00000530012.1:n.297G=
ENST00000531756.5:n.1017G=
ENST00000532236.5:c.1122G=	ENSP00000434112.1:p.Met374=
NM_001145211.2:c.1404G=	NP_001138683.1:p.Met468=
NM_001145212.2:c.1038G=	NP_001138684.1:p.Met346=
NM_007256.4:c.1470G=	NP_009187.1:p.Met490=
XM_017017157.1:c.1476G=	XP_016872646.1:p.Met492=
NM_001145211.3:c.1404G=	NP_001138683.1:p.Met468=
NM_001145212.3:c.1038G=	NP_001138684.1:p.Met346=
NM_007256.5:c.1470G= MANE Select	NP_009187.1:p.Met490=