Canonical Allele Identifier: CA233565050
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs186601252
gnomAD v2: 12-21368125-C-T
gnomAD v3: 12-21215191-C-T
gnomAD v4: 12-21215191-C-T
MyVariant Identifiers: chr12:g.21368125C>T (hg19) chr12:g.21215191C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21215191C>T , CM000674.2:g.21215191C>T GRCh38
NC_000012.11:g.21368125C>T , CM000674.1:g.21368125C>T GRCh37
NC_000012.10:g.21259392C>T NCBI36
NG_011745.1:g.88998C>T , LRG_1022:g.88998C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.1498-1928C>T MANE Select ENSP00000256958.2:n.1498-1928C>T
ENST00000256958.2:c.1498-1928C>T ENSP00000256958.2:n.1498-1928C>T
NM_006446.4:c.1498-1928C>T , LRG_1022t1:c.1498-1928C>T NP_006437.3:n.1498-1928C>T
NM_006446.5:c.1498-1928C>T MANE Select NP_006437.3:n.1498-1928C>T
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