Canonical Allele Identifier: CA381871135

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907590T>A (hg19) ; chr11:g.75196545T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196545T>A , CM000673.2:g.75196545T>A	GRCh38
NC_000011.9:g.74907590T>A , CM000673.1:g.74907590T>A	GRCh37
NC_000011.8:g.74585238T>A	NCBI36
NG_027921.1:g.50559T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1465T>A MANE Select	ENSP00000289575.5:p.Cys489Ser
ENST00000289575.9:c.1465T>A	ENSP00000289575.5:p.Cys489Ser
ENST00000428359.6:c.1399T>A	ENSP00000388912.2:p.Cys467Ser
ENST00000454962.6:c.784T>A	ENSP00000389653.2:p.Cys262Ser
ENST00000525650.5:c.1033T>A	ENSP00000436324.1:p.Cys345Ser
ENST00000528108.1:n.271T>A
ENST00000530012.1:n.292T>A
ENST00000531756.5:n.1012T>A
ENST00000532236.5:c.1117T>A	ENSP00000434112.1:p.Cys373Ser
NM_001145211.2:c.1399T>A	NP_001138683.1:p.Cys467Ser
NM_001145212.2:c.1033T>A	NP_001138684.1:p.Cys345Ser
NM_007256.4:c.1465T>A	NP_009187.1:p.Cys489Ser
XM_017017157.1:c.1471T>A	XP_016872646.1:p.Cys491Ser
NM_001145211.3:c.1399T>A	NP_001138683.1:p.Cys467Ser
NM_001145212.3:c.1033T>A	NP_001138684.1:p.Cys345Ser
NM_007256.5:c.1465T>A MANE Select	NP_009187.1:p.Cys489Ser