Canonical Allele Identifier: CA381871133

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907589C>A (hg19) ; chr11:g.75196544C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196544C>A , CM000673.2:g.75196544C>A	GRCh38
NC_000011.9:g.74907589C>A , CM000673.1:g.74907589C>A	GRCh37
NC_000011.8:g.74585237C>A	NCBI36
NG_027921.1:g.50558C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1464C>A MANE Select	ENSP00000289575.5:p.Ser488Arg
ENST00000289575.9:c.1464C>A	ENSP00000289575.5:p.Ser488Arg
ENST00000428359.6:c.1398C>A	ENSP00000388912.2:p.Ser466Arg
ENST00000454962.6:c.783C>A	ENSP00000389653.2:p.Ser261Arg
ENST00000525650.5:c.1032C>A	ENSP00000436324.1:p.Ser344Arg
ENST00000528108.1:n.270C>A
ENST00000530012.1:n.291C>A
ENST00000531756.5:n.1011C>A
ENST00000532236.5:c.1116C>A	ENSP00000434112.1:p.Ser372Arg
NM_001145211.2:c.1398C>A	NP_001138683.1:p.Ser466Arg
NM_001145212.2:c.1032C>A	NP_001138684.1:p.Ser344Arg
NM_007256.4:c.1464C>A	NP_009187.1:p.Ser488Arg
XM_017017157.1:c.1470C>A	XP_016872646.1:p.Ser490Arg
NM_001145211.3:c.1398C>A	NP_001138683.1:p.Ser466Arg
NM_001145212.3:c.1032C>A	NP_001138684.1:p.Ser344Arg
NM_007256.5:c.1464C>A MANE Select	NP_009187.1:p.Ser488Arg