Canonical Allele Identifier: CA381871146

Gene: SLCO2B1

Linked Data

• gnomAD v4: 11-75196549-T-C
• MyVariant Identifiers: chr11:g.74907594T>C (hg19) ; chr11:g.75196549T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196549T>C , CM000673.2:g.75196549T>C	GRCh38
NC_000011.9:g.74907594T>C , CM000673.1:g.74907594T>C	GRCh37
NC_000011.8:g.74585242T>C	NCBI36
NG_027921.1:g.50563T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1469T>C MANE Select	ENSP00000289575.5:p.Met490Thr
ENST00000289575.9:c.1469T>C	ENSP00000289575.5:p.Met490Thr
ENST00000428359.6:c.1403T>C	ENSP00000388912.2:p.Met468Thr
ENST00000454962.6:c.788T>C	ENSP00000389653.2:p.Met263Thr
ENST00000525650.5:c.1037T>C	ENSP00000436324.1:p.Met346Thr
ENST00000528108.1:n.275T>C
ENST00000530012.1:n.296T>C
ENST00000531756.5:n.1016T>C
ENST00000532236.5:c.1121T>C	ENSP00000434112.1:p.Met374Thr
NM_001145211.2:c.1403T>C	NP_001138683.1:p.Met468Thr
NM_001145212.2:c.1037T>C	NP_001138684.1:p.Met346Thr
NM_007256.4:c.1469T>C	NP_009187.1:p.Met490Thr
XM_017017157.1:c.1475T>C	XP_016872646.1:p.Met492Thr
NM_001145211.3:c.1403T>C	NP_001138683.1:p.Met468Thr
NM_001145212.3:c.1037T>C	NP_001138684.1:p.Met346Thr
NM_007256.5:c.1469T>C MANE Select	NP_009187.1:p.Met490Thr