Canonical Allele Identifier: CA603657582
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1266631570
gnomAD v2: 12-21327413-A-G
gnomAD v3: 12-21174479-A-G
gnomAD v4: 12-21174479-A-G
MyVariant Identifiers: chr12:g.21327413A>G (hg19) chr12:g.21174479A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174479A>G , CM000674.2:g.21174479A>G GRCh38
NC_000012.11:g.21327413A>G , CM000674.1:g.21327413A>G GRCh37
NC_000012.10:g.21218680A>G NCBI36
NG_011745.1:g.48286A>G , LRG_1022:g.48286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.227-98A>G MANE Select ENSP00000256958.2:n.227-98A>G
ENST00000256958.2:c.227-98A>G ENSP00000256958.2:n.227-98A>G
ENST00000543498.5:c.426-2297A>G
NM_006446.4:c.227-98A>G , LRG_1022t1:c.227-98A>G NP_006437.3:n.227-98A>G
NM_006446.5:c.227-98A>G MANE Select NP_006437.3:n.227-98A>G
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