Canonical Allele Identifier: CA10632369
Gene: SLCO1B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 307884
ClinVar RCV Id: RCV000274757
dbSNP Id: rs7305323
gnomAD v2: 12-20966548-C-T
gnomAD v3: 12-20813614-C-T
gnomAD v4: 12-20813614-C-T
MyVariant Identifiers: chr12:g.20966548C>T (hg19) chr12:g.20813614C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20813614C>T , CM000674.2:g.20813614C>T GRCh38
NC_000012.11:g.20966548C>T , CM000674.1:g.20966548C>T GRCh37
NC_000012.10:g.20857815C>T NCBI36
NG_032071.1:g.7911C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381545.8:c.-90C>T MANE Select ENSP00000370956.4:n.-90C>T
ENST00000381545.7:c.-90C>T ENSP00000370956.3:n.-90C>T
ENST00000540853.5:c.-65-2060C>T ENSP00000442000.1:n.-65-2060C>T
NM_019844.3:c.-90C>T NP_062818.1:n.-90C>T
NM_019844.4:c.-90C>T MANE Select NP_062818.1:n.-90C>T
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