Canonical Allele Identifier: CA384104357
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1375717172

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174695T>G , CM000674.2:g.21174695T>G GRCh38
NC_000012.11:g.21327629T>G , CM000674.1:g.21327629T>G GRCh37
NC_000012.10:g.21218896T>G NCBI36
NG_011745.1:g.48502T>G , LRG_1022:g.48502T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.345T>G MANE Select ENSP00000256958.2:p.His115Gln
ENST00000256958.2:c.345T>G ENSP00000256958.2:p.His115Gln
ENST00000543498.5:c.426-2081T>G
NM_006446.4:c.345T>G , LRG_1022t1:c.345T>G NP_006437.3:p.His115Gln
NM_006446.5:c.345T>G MANE Select NP_006437.3:p.His115Gln