Canonical Allele Identifier: CA478866550
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1940797052
gnomAD v4: 12-21174635-G-A
MyVariant Identifiers: chr12:g.21327569G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174635G>A , CM000674.2:g.21174635G>A GRCh38
NC_000012.11:g.21327569G>A , CM000674.1:g.21327569G>A GRCh37
NC_000012.10:g.21218836G>A NCBI36
NG_011745.1:g.48442G>A , LRG_1022:g.48442G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.285G>A MANE Select ENSP00000256958.2:p.Lys95=
ENST00000256958.2:c.285G>A ENSP00000256958.2:p.Lys95=
ENST00000543498.5:c.426-2141G>A
NM_006446.4:c.285G>A , LRG_1022t1:c.285G>A NP_006437.3:p.Lys95=
NM_006446.5:c.285G>A MANE Select NP_006437.3:p.Lys95=
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