Canonical Allele Identifier: CA478866907
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21329809A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176875A>G , CM000674.2:g.21176875A>G GRCh38
NC_000012.11:g.21329809A>G , CM000674.1:g.21329809A>G GRCh37
NC_000012.10:g.21221076A>G NCBI36
NG_011745.1:g.50682A>G , LRG_1022:g.50682A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.459A>G MANE Select ENSP00000256958.2:p.Ala153=
ENST00000256958.2:c.459A>G ENSP00000256958.2:p.Ala153=
ENST00000543498.5:c.525A>G
NM_006446.4:c.459A>G , LRG_1022t1:c.459A>G NP_006437.3:p.Ala153=
NM_006446.5:c.459A>G MANE Select NP_006437.3:p.Ala153=