Canonical Allele Identifier: CA686354221
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1323223484
gnomAD v4: 12-21176684-G-A
MyVariant Identifiers: chr12:g.21329618G>A (hg19) chr12:g.21176684G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21176684G>A , CM000674.2:g.21176684G>A GRCh38
NC_000012.11:g.21329618G>A , CM000674.1:g.21329618G>A GRCh37
NC_000012.10:g.21220885G>A NCBI36
NG_011745.1:g.50491G>A , LRG_1022:g.50491G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.360-92G>A MANE Select ENSP00000256958.2:n.360-92G>A
ENST00000256958.2:c.360-92G>A ENSP00000256958.2:n.360-92G>A
ENST00000543498.5:c.426-92G>A
NM_006446.4:c.360-92G>A , LRG_1022t1:c.360-92G>A NP_006437.3:n.360-92G>A
NM_006446.5:c.360-92G>A MANE Select NP_006437.3:n.360-92G>A
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