Canonical Allele Identifier: CA475707492

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907586A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196541A>G , CM000673.2:g.75196541A>G	GRCh38
NC_000011.9:g.74907586A>G , CM000673.1:g.74907586A>G	GRCh37
NC_000011.8:g.74585234A>G	NCBI36
NG_027921.1:g.50555A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1461A>G MANE Select	ENSP00000289575.5:p.Pro487=
ENST00000289575.9:c.1461A>G	ENSP00000289575.5:p.Pro487=
ENST00000428359.6:c.1395A>G	ENSP00000388912.2:p.Pro465=
ENST00000454962.6:c.780A>G	ENSP00000389653.2:p.Pro260=
ENST00000525650.5:c.1029A>G	ENSP00000436324.1:p.Pro343=
ENST00000528108.1:n.267A>G
ENST00000530012.1:n.288A>G
ENST00000531756.5:n.1008A>G
ENST00000532236.5:c.1113A>G	ENSP00000434112.1:p.Pro371=
NM_001145211.2:c.1395A>G	NP_001138683.1:p.Pro465=
NM_001145212.2:c.1029A>G	NP_001138684.1:p.Pro343=
NM_007256.4:c.1461A>G	NP_009187.1:p.Pro487=
XM_017017157.1:c.1467A>G	XP_016872646.1:p.Pro489=
NM_001145211.3:c.1395A>G	NP_001138683.1:p.Pro465=
NM_001145212.3:c.1029A>G	NP_001138684.1:p.Pro343=
NM_007256.5:c.1461A>G MANE Select	NP_009187.1:p.Pro487=