Canonical Allele Identifier: CA233560886
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs756788386

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176782G>A , CM000674.2:g.21176782G>A GRCh38
NC_000012.11:g.21329716G>A , CM000674.1:g.21329716G>A GRCh37
NC_000012.10:g.21220983G>A NCBI36
NG_011745.1:g.50589G>A , LRG_1022:g.50589G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.366G>A MANE Select ENSP00000256958.2:p.Arg122=
ENST00000256958.2:c.366G>A ENSP00000256958.2:p.Arg122=
ENST00000543498.5:c.432G>A
NM_006446.4:c.366G>A , LRG_1022t1:c.366G>A NP_006437.3:p.Arg122=
NM_006446.5:c.366G>A MANE Select NP_006437.3:p.Arg122=