Canonical Allele Identifier: CA475707501

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907589C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1464C>T MANE Select	ENSP00000289575.5:p.Ser488=
ENST00000289575.9:c.1464C>T	ENSP00000289575.5:p.Ser488=
ENST00000428359.6:c.1398C>T	ENSP00000388912.2:p.Ser466=
ENST00000454962.6:c.783C>T	ENSP00000389653.2:p.Ser261=
ENST00000525650.5:c.1032C>T	ENSP00000436324.1:p.Ser344=
ENST00000528108.1:n.270C>T
ENST00000530012.1:n.291C>T
ENST00000531756.5:n.1011C>T
ENST00000532236.5:c.1116C>T	ENSP00000434112.1:p.Ser372=
NM_001145211.2:c.1398C>T	NP_001138683.1:p.Ser466=
NM_001145212.2:c.1032C>T	NP_001138684.1:p.Ser344=
NM_007256.4:c.1464C>T	NP_009187.1:p.Ser488=
XM_017017157.1:c.1470C>T	XP_016872646.1:p.Ser490=
NM_001145211.3:c.1398C>T	NP_001138683.1:p.Ser466=
NM_001145212.3:c.1032C>T	NP_001138684.1:p.Ser344=
NM_007256.5:c.1464C>T MANE Select	NP_009187.1:p.Ser488=