Canonical Allele Identifier: CA381871132

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907588G>T (hg19) ; chr11:g.75196543G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196543G>T , CM000673.2:g.75196543G>T	GRCh38
NC_000011.9:g.74907588G>T , CM000673.1:g.74907588G>T	GRCh37
NC_000011.8:g.74585236G>T	NCBI36
NG_027921.1:g.50557G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1463G>T MANE Select	ENSP00000289575.5:p.Ser488Ile
ENST00000289575.9:c.1463G>T	ENSP00000289575.5:p.Ser488Ile
ENST00000428359.6:c.1397G>T	ENSP00000388912.2:p.Ser466Ile
ENST00000454962.6:c.782G>T	ENSP00000389653.2:p.Ser261Ile
ENST00000525650.5:c.1031G>T	ENSP00000436324.1:p.Ser344Ile
ENST00000528108.1:n.269G>T
ENST00000530012.1:n.290G>T
ENST00000531756.5:n.1010G>T
ENST00000532236.5:c.1115G>T	ENSP00000434112.1:p.Ser372Ile
NM_001145211.2:c.1397G>T	NP_001138683.1:p.Ser466Ile
NM_001145212.2:c.1031G>T	NP_001138684.1:p.Ser344Ile
NM_007256.4:c.1463G>T	NP_009187.1:p.Ser488Ile
XM_017017157.1:c.1469G>T	XP_016872646.1:p.Ser490Ile
NM_001145211.3:c.1397G>T	NP_001138683.1:p.Ser466Ile
NM_001145212.3:c.1031G>T	NP_001138684.1:p.Ser344Ile
NM_007256.5:c.1463G>T MANE Select	NP_009187.1:p.Ser488Ile