Canonical Allele Identifier: CA381871124

Gene: SLCO2B1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1460C>G MANE Select	ENSP00000289575.5:p.Pro487Arg
ENST00000289575.9:c.1460C>G	ENSP00000289575.5:p.Pro487Arg
ENST00000428359.6:c.1394C>G	ENSP00000388912.2:p.Pro465Arg
ENST00000454962.6:c.779C>G	ENSP00000389653.2:p.Pro260Arg
ENST00000525650.5:c.1028C>G	ENSP00000436324.1:p.Pro343Arg
ENST00000528108.1:n.266C>G
ENST00000530012.1:n.287C>G
ENST00000531756.5:n.1007C>G
ENST00000532236.5:c.1112C>G	ENSP00000434112.1:p.Pro371Arg
NM_001145211.2:c.1394C>G	NP_001138683.1:p.Pro465Arg
NM_001145212.2:c.1028C>G	NP_001138684.1:p.Pro343Arg
NM_007256.4:c.1460C>G	NP_009187.1:p.Pro487Arg
XM_017017157.1:c.1466C>G	XP_016872646.1:p.Pro489Arg
NM_001145211.3:c.1394C>G	NP_001138683.1:p.Pro465Arg
NM_001145212.3:c.1028C>G	NP_001138684.1:p.Pro343Arg
NM_007256.5:c.1460C>G MANE Select	NP_009187.1:p.Pro487Arg