Canonical Allele Identifier: CA686353434
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1385385036
gnomAD v3: 12-21175059-G-T
gnomAD v4: 12-21175059-G-T
MyVariant Identifiers: chr12:g.21327993G>T (hg19) chr12:g.21175059G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21175059G>T , CM000674.2:g.21175059G>T GRCh38
NC_000012.11:g.21327993G>T , CM000674.1:g.21327993G>T GRCh37
NC_000012.10:g.21219260G>T NCBI36
NG_011745.1:g.48866G>T , LRG_1022:g.48866G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.359+350G>T MANE Select ENSP00000256958.2:n.359+350G>T
ENST00000256958.2:c.359+350G>T ENSP00000256958.2:n.359+350G>T
ENST00000543498.5:c.426-1717G>T
NM_006446.4:c.359+350G>T , LRG_1022t1:c.359+350G>T NP_006437.3:n.359+350G>T
NM_006446.5:c.359+350G>T MANE Select NP_006437.3:n.359+350G>T
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