Canonical Allele Identifier: CA686354267
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1188901027
gnomAD v3: 12-21176764-A-G
gnomAD v4: 12-21176764-A-G
MyVariant Identifiers: chr12:g.21329698A>G (hg19) chr12:g.21176764A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176764A>G , CM000674.2:g.21176764A>G GRCh38
NC_000012.11:g.21329698A>G , CM000674.1:g.21329698A>G GRCh37
NC_000012.10:g.21220965A>G NCBI36
NG_011745.1:g.50571A>G , LRG_1022:g.50571A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.360-12A>G MANE Select ENSP00000256958.2:n.360-12A>G
ENST00000256958.2:c.360-12A>G ENSP00000256958.2:n.360-12A>G
ENST00000543498.5:c.426-12A>G
NM_006446.4:c.360-12A>G , LRG_1022t1:c.360-12A>G NP_006437.3:n.360-12A>G
NM_006446.5:c.360-12A>G MANE Select NP_006437.3:n.360-12A>G
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