Canonical Allele Identifier: CA2020999852
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs927005981
gnomAD v4: 12-21196934-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21196934T>A , CM000674.2:g.21196934T>A GRCh38
NC_000012.11:g.21349868T>A , CM000674.1:g.21349868T>A GRCh37
NC_000012.10:g.21241135T>A NCBI36
NG_011745.1:g.70741T>A , LRG_1022:g.70741T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.728-12T>A MANE Select ENSP00000256958.2:n.728-12T>A
ENST00000256958.2:c.728-12T>A ENSP00000256958.2:n.728-12T>A
NM_006446.4:c.728-12T>A , LRG_1022t1:c.728-12T>A NP_006437.3:n.728-12T>A
NM_006446.5:c.728-12T>A MANE Select NP_006437.3:n.728-12T>A
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