Canonical Allele Identifier: CA384106819
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21200663-A-G
MyVariant Identifiers: chr12:g.21353597A>G (hg19) chr12:g.21200663A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200663A>G , CM000674.2:g.21200663A>G GRCh38
NC_000012.11:g.21353597A>G , CM000674.1:g.21353597A>G GRCh37
NC_000012.10:g.21244864A>G NCBI36
NG_011745.1:g.74470A>G , LRG_1022:g.74470A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1126A>G MANE Select ENSP00000256958.2:p.Ile376Val
ENST00000256958.2:c.1126A>G ENSP00000256958.2:p.Ile376Val
NM_006446.4:c.1126A>G , LRG_1022t1:c.1126A>G NP_006437.3:p.Ile376Val
NM_006446.5:c.1126A>G MANE Select NP_006437.3:p.Ile376Val
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