Canonical Allele Identifier: CA603656079
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1402633270
gnomAD v2: 12-21291504-A-G
gnomAD v3: 12-21138570-A-G
gnomAD v4: 12-21138570-A-G
MyVariant Identifiers: chr12:g.21291504A>G (hg19) chr12:g.21138570A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21138570A>G , CM000674.2:g.21138570A>G GRCh38
NC_000012.11:g.21291504A>G , CM000674.1:g.21291504A>G GRCh37
NC_000012.10:g.21182771A>G NCBI36
NG_011745.1:g.12377A>G , LRG_1022:g.12377A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.-61-2944A>G MANE Select ENSP00000256958.2:n.-61-2944A>G
ENST00000256958.2:c.-61-2944A>G ENSP00000256958.2:n.-61-2944A>G
ENST00000543498.5:c.281-2944A>G
ENST00000585342.5:c.485-2944A>G ENSP00000467594.1:n.485-2944A>G
ENST00000590779.5:c.491-2944A>G
ENST00000592513.1:c.472-2944A>G
NM_006446.4:c.-61-2944A>G , LRG_1022t1:c.-61-2944A>G NP_006437.3:n.-61-2944A>G
NM_006446.5:c.-61-2944A>G MANE Select NP_006437.3:n.-61-2944A>G
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