Canonical Allele Identifier: CA381871126

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907585C>A (hg19) ; chr11:g.75196540C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196540C>A , CM000673.2:g.75196540C>A	GRCh38
NC_000011.9:g.74907585C>A , CM000673.1:g.74907585C>A	GRCh37
NC_000011.8:g.74585233C>A	NCBI36
NG_027921.1:g.50554C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1460C>A MANE Select	ENSP00000289575.5:p.Pro487Gln
ENST00000289575.9:c.1460C>A	ENSP00000289575.5:p.Pro487Gln
ENST00000428359.6:c.1394C>A	ENSP00000388912.2:p.Pro465Gln
ENST00000454962.6:c.779C>A	ENSP00000389653.2:p.Pro260Gln
ENST00000525650.5:c.1028C>A	ENSP00000436324.1:p.Pro343Gln
ENST00000528108.1:n.266C>A
ENST00000530012.1:n.287C>A
ENST00000531756.5:n.1007C>A
ENST00000532236.5:c.1112C>A	ENSP00000434112.1:p.Pro371Gln
NM_001145211.2:c.1394C>A	NP_001138683.1:p.Pro465Gln
NM_001145212.2:c.1028C>A	NP_001138684.1:p.Pro343Gln
NM_007256.4:c.1460C>A	NP_009187.1:p.Pro487Gln
XM_017017157.1:c.1466C>A	XP_016872646.1:p.Pro489Gln
NM_001145211.3:c.1394C>A	NP_001138683.1:p.Pro465Gln
NM_001145212.3:c.1028C>A	NP_001138684.1:p.Pro343Gln
NM_007256.5:c.1460C>A MANE Select	NP_009187.1:p.Pro487Gln