Canonical Allele Identifier: CA945475905
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1941142613
gnomAD v3: 12-21200401-G-A
gnomAD v4: 12-21200401-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21200401G>A , CM000674.2:g.21200401G>A GRCh38
NC_000012.11:g.21353335G>A , CM000674.1:g.21353335G>A GRCh37
NC_000012.10:g.21244602G>A NCBI36
NG_011745.1:g.74208G>A , LRG_1022:g.74208G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.971-107G>A MANE Select ENSP00000256958.2:n.971-107G>A
ENST00000256958.2:c.971-107G>A ENSP00000256958.2:n.971-107G>A
NM_006446.4:c.971-107G>A , LRG_1022t1:c.971-107G>A NP_006437.3:n.971-107G>A
NM_006446.5:c.971-107G>A MANE Select NP_006437.3:n.971-107G>A
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