Canonical Allele Identifier: CA384105520
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21178624-G-A
MyVariant Identifiers: chr12:g.21331558G>A (hg19) chr12:g.21178624G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178624G>A , CM000674.2:g.21178624G>A GRCh38
NC_000012.11:g.21331558G>A , CM000674.1:g.21331558G>A GRCh37
NC_000012.10:g.21222825G>A NCBI36
NG_011745.1:g.52431G>A , LRG_1022:g.52431G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.530G>A MANE Select ENSP00000256958.2:p.Gly177Asp
ENST00000256958.2:c.530G>A ENSP00000256958.2:p.Gly177Asp
NM_006446.4:c.530G>A , LRG_1022t1:c.530G>A NP_006437.3:p.Gly177Asp
NM_006446.5:c.530G>A MANE Select NP_006437.3:p.Gly177Asp
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