Canonical Allele Identifier: CA381871122

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907584C>A (hg19) ; chr11:g.75196539C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196539C>A , CM000673.2:g.75196539C>A	GRCh38
NC_000011.9:g.74907584C>A , CM000673.1:g.74907584C>A	GRCh37
NC_000011.8:g.74585232C>A	NCBI36
NG_027921.1:g.50553C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1459C>A MANE Select	ENSP00000289575.5:p.Pro487Thr
ENST00000289575.9:c.1459C>A	ENSP00000289575.5:p.Pro487Thr
ENST00000428359.6:c.1393C>A	ENSP00000388912.2:p.Pro465Thr
ENST00000454962.6:c.778C>A	ENSP00000389653.2:p.Pro260Thr
ENST00000525650.5:c.1027C>A	ENSP00000436324.1:p.Pro343Thr
ENST00000528108.1:n.265C>A
ENST00000530012.1:n.286C>A
ENST00000531756.5:n.1006C>A
ENST00000532236.5:c.1111C>A	ENSP00000434112.1:p.Pro371Thr
NM_001145211.2:c.1393C>A	NP_001138683.1:p.Pro465Thr
NM_001145212.2:c.1027C>A	NP_001138684.1:p.Pro343Thr
NM_007256.4:c.1459C>A	NP_009187.1:p.Pro487Thr
XM_017017157.1:c.1465C>A	XP_016872646.1:p.Pro489Thr
NM_001145211.3:c.1393C>A	NP_001138683.1:p.Pro465Thr
NM_001145212.3:c.1027C>A	NP_001138684.1:p.Pro343Thr
NM_007256.5:c.1459C>A MANE Select	NP_009187.1:p.Pro487Thr