Canonical Allele Identifier: CA384105512
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178620A>G , CM000674.2:g.21178620A>G GRCh38
NC_000012.11:g.21331554A>G , CM000674.1:g.21331554A>G GRCh37
NC_000012.10:g.21222821A>G NCBI36
NG_011745.1:g.52427A>G , LRG_1022:g.52427A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.526A>G MANE Select ENSP00000256958.2:p.Met176Val
ENST00000256958.2:c.526A>G ENSP00000256958.2:p.Met176Val
NM_006446.4:c.526A>G , LRG_1022t1:c.526A>G NP_006437.3:p.Met176Val
NM_006446.5:c.526A>G MANE Select NP_006437.3:p.Met176Val