Canonical Allele Identifier: CA478866630
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21174686-T-C
MyVariant Identifiers: chr12:g.21327620T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174686T>C , CM000674.2:g.21174686T>C GRCh38
NC_000012.11:g.21327620T>C , CM000674.1:g.21327620T>C GRCh37
NC_000012.10:g.21218887T>C NCBI36
NG_011745.1:g.48493T>C , LRG_1022:g.48493T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.336T>C MANE Select ENSP00000256958.2:p.Ala112=
ENST00000256958.2:c.336T>C ENSP00000256958.2:p.Ala112=
ENST00000543498.5:c.426-2090T>C
NM_006446.4:c.336T>C , LRG_1022t1:c.336T>C NP_006437.3:p.Ala112=
NM_006446.5:c.336T>C MANE Select NP_006437.3:p.Ala112=
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Search 100 bp 3'