Canonical Allele Identifier: CA1983217962

Gene: SLCO2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196445G= , CM000673.2:g.75196445G=	GRCh38
NC_000011.9:g.74907490G= , CM000673.1:g.74907490G=	GRCh37
NC_000011.8:g.74585138G=	NCBI36
NG_027921.1:g.50459G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1434-69G= MANE Select	ENSP00000289575.5:n.1434-69G=
ENST00000289575.9:c.1434-69G=	ENSP00000289575.5:n.1434-69G=
ENST00000428359.6:c.1368-69G=	ENSP00000388912.2:n.1368-69G=
ENST00000454962.6:c.753-69G=	ENSP00000389653.2:n.753-69G=
ENST00000525650.5:c.1002-69G=	ENSP00000436324.1:n.1002-69G=
ENST00000528108.1:n.171G=
ENST00000530012.1:n.192G=
ENST00000531756.5:n.981-69G=
ENST00000532236.5:c.1086-69G=	ENSP00000434112.1:n.1086-69G=
NM_001145211.2:c.1368-69G=	NP_001138683.1:n.1368-69G=
NM_001145212.2:c.1002-69G=	NP_001138684.1:n.1002-69G=
NM_007256.4:c.1434-69G=	NP_009187.1:n.1434-69G=
XM_017017157.1:c.1440-69G=	XP_016872646.1:n.1440-69G=
NM_001145211.3:c.1368-69G=	NP_001138683.1:n.1368-69G=
NM_001145212.3:c.1002-69G=	NP_001138684.1:n.1002-69G=
NM_007256.5:c.1434-69G= MANE Select	NP_009187.1:n.1434-69G=