Canonical Allele Identifier: CA475707477

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907583T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196538T>C , CM000673.2:g.75196538T>C	GRCh38
NC_000011.9:g.74907583T>C , CM000673.1:g.74907583T>C	GRCh37
NC_000011.8:g.74585231T>C	NCBI36
NG_027921.1:g.50552T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1458T>C MANE Select	ENSP00000289575.5:p.Ser486=
ENST00000289575.9:c.1458T>C	ENSP00000289575.5:p.Ser486=
ENST00000428359.6:c.1392T>C	ENSP00000388912.2:p.Ser464=
ENST00000454962.6:c.777T>C	ENSP00000389653.2:p.Ser259=
ENST00000525650.5:c.1026T>C	ENSP00000436324.1:p.Ser342=
ENST00000528108.1:n.264T>C
ENST00000530012.1:n.285T>C
ENST00000531756.5:n.1005T>C
ENST00000532236.5:c.1110T>C	ENSP00000434112.1:p.Ser370=
NM_001145211.2:c.1392T>C	NP_001138683.1:p.Ser464=
NM_001145212.2:c.1026T>C	NP_001138684.1:p.Ser342=
NM_007256.4:c.1458T>C	NP_009187.1:p.Ser486=
XM_017017157.1:c.1464T>C	XP_016872646.1:p.Ser488=
NM_001145211.3:c.1392T>C	NP_001138683.1:p.Ser464=
NM_001145212.3:c.1026T>C	NP_001138684.1:p.Ser342=
NM_007256.5:c.1458T>C MANE Select	NP_009187.1:p.Ser486=