Canonical Allele Identifier: CA384104281
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21174676-T-A
MyVariant Identifiers: chr12:g.21327610T>A (hg19) chr12:g.21174676T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174676T>A , CM000674.2:g.21174676T>A GRCh38
NC_000012.11:g.21327610T>A , CM000674.1:g.21327610T>A GRCh37
NC_000012.10:g.21218877T>A NCBI36
NG_011745.1:g.48483T>A , LRG_1022:g.48483T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.326T>A MANE Select ENSP00000256958.2:p.Val109Asp
ENST00000256958.2:c.326T>A ENSP00000256958.2:p.Val109Asp
ENST00000543498.5:c.426-2100T>A
NM_006446.4:c.326T>A , LRG_1022t1:c.326T>A NP_006437.3:p.Val109Asp
NM_006446.5:c.326T>A MANE Select NP_006437.3:p.Val109Asp
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