Canonical Allele Identifier: CA2617895111
Gene: SLCO1B1 HGNC NCBI

Linked Data

gnomAD v4: 12-21174558-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174558A>T , CM000674.2:g.21174558A>T GRCh38
NC_000012.11:g.21327492A>T , CM000674.1:g.21327492A>T GRCh37
NC_000012.10:g.21218759A>T NCBI36
NG_011745.1:g.48365A>T , LRG_1022:g.48365A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227-19A>T MANE Select ENSP00000256958.2:n.227-19A>T
ENST00000256958.2:c.227-19A>T ENSP00000256958.2:n.227-19A>T
ENST00000543498.5:c.426-2218A>T
NM_006446.4:c.227-19A>T , LRG_1022t1:c.227-19A>T NP_006437.3:n.227-19A>T
NM_006446.5:c.227-19A>T MANE Select NP_006437.3:n.227-19A>T
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