Canonical Allele Identifier: CA2020989583
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1667242082
gnomAD v4: 12-21174525-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174525T>A , CM000674.2:g.21174525T>A GRCh38
NC_000012.11:g.21327459T>A , CM000674.1:g.21327459T>A GRCh37
NC_000012.10:g.21218726T>A NCBI36
NG_011745.1:g.48332T>A , LRG_1022:g.48332T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.227-52T>A MANE Select ENSP00000256958.2:n.227-52T>A
ENST00000256958.2:c.227-52T>A ENSP00000256958.2:n.227-52T>A
ENST00000543498.5:c.426-2251T>A
NM_006446.4:c.227-52T>A , LRG_1022t1:c.227-52T>A NP_006437.3:n.227-52T>A
NM_006446.5:c.227-52T>A MANE Select NP_006437.3:n.227-52T>A
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