Canonical Allele Identifier: CA381871149

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907595G>C (hg19) ; chr11:g.75196550G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196550G>C , CM000673.2:g.75196550G>C	GRCh38
NC_000011.9:g.74907595G>C , CM000673.1:g.74907595G>C	GRCh37
NC_000011.8:g.74585243G>C	NCBI36
NG_027921.1:g.50564G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1470G>C MANE Select	ENSP00000289575.5:p.Met490Ile
ENST00000289575.9:c.1470G>C	ENSP00000289575.5:p.Met490Ile
ENST00000428359.6:c.1404G>C	ENSP00000388912.2:p.Met468Ile
ENST00000454962.6:c.789G>C	ENSP00000389653.2:p.Met263Ile
ENST00000525650.5:c.1038G>C	ENSP00000436324.1:p.Met346Ile
ENST00000528108.1:n.276G>C
ENST00000530012.1:n.297G>C
ENST00000531756.5:n.1017G>C
ENST00000532236.5:c.1122G>C	ENSP00000434112.1:p.Met374Ile
NM_001145211.2:c.1404G>C	NP_001138683.1:p.Met468Ile
NM_001145212.2:c.1038G>C	NP_001138684.1:p.Met346Ile
NM_007256.4:c.1470G>C	NP_009187.1:p.Met490Ile
XM_017017157.1:c.1476G>C	XP_016872646.1:p.Met492Ile
NM_001145211.3:c.1404G>C	NP_001138683.1:p.Met468Ile
NM_001145212.3:c.1038G>C	NP_001138684.1:p.Met346Ile
NM_007256.5:c.1470G>C MANE Select	NP_009187.1:p.Met490Ile