Canonical Allele Identifier: CA6476903
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs769283535
COSMIC: COSM468129

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200598G>A , CM000674.2:g.21200598G>A GRCh38
NC_000012.11:g.21353532G>A , CM000674.1:g.21353532G>A GRCh37
NC_000012.10:g.21244799G>A NCBI36
NG_011745.1:g.74405G>A , LRG_1022:g.74405G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.1061G>A MANE Select ENSP00000256958.2:p.Gly354Asp
ENST00000256958.2:c.1061G>A ENSP00000256958.2:p.Gly354Asp
NM_006446.4:c.1061G>A , LRG_1022t1:c.1061G>A NP_006437.3:p.Gly354Asp
NM_006446.5:c.1061G>A MANE Select NP_006437.3:p.Gly354Asp