Canonical Allele Identifier: CA478866541
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21327566A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174632A>C , CM000674.2:g.21174632A>C GRCh38
NC_000012.11:g.21327566A>C , CM000674.1:g.21327566A>C GRCh37
NC_000012.10:g.21218833A>C NCBI36
NG_011745.1:g.48439A>C , LRG_1022:g.48439A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.282A>C MANE Select ENSP00000256958.2:p.Pro94=
ENST00000256958.2:c.282A>C ENSP00000256958.2:p.Pro94=
ENST00000543498.5:c.426-2144A>C
NM_006446.4:c.282A>C , LRG_1022t1:c.282A>C NP_006437.3:p.Pro94=
NM_006446.5:c.282A>C MANE Select NP_006437.3:p.Pro94=