Canonical Allele Identifier: CA384105558
Gene: SLCO1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.21331576T>C (hg19) chr12:g.21178642T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178642T>C , CM000674.2:g.21178642T>C GRCh38
NC_000012.11:g.21331576T>C , CM000674.1:g.21331576T>C GRCh37
NC_000012.10:g.21222843T>C NCBI36
NG_011745.1:g.52449T>C , LRG_1022:g.52449T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.548T>C MANE Select ENSP00000256958.2:p.Ile183Thr
ENST00000256958.2:c.548T>C ENSP00000256958.2:p.Ile183Thr
NM_006446.4:c.548T>C , LRG_1022t1:c.548T>C NP_006437.3:p.Ile183Thr
NM_006446.5:c.548T>C MANE Select NP_006437.3:p.Ile183Thr
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