Canonical Allele Identifier: CA6476627
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs755571702
ExAC: 12:21327497 T / A
gnomAD v2: 12-21327497-T-A
gnomAD v4: 12-21174563-T-A
MyVariant Identifiers: chr12:g.21327497T>A (hg19) chr12:g.21174563T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174563T>A , CM000674.2:g.21174563T>A GRCh38
NC_000012.11:g.21327497T>A , CM000674.1:g.21327497T>A GRCh37
NC_000012.10:g.21218764T>A NCBI36
NG_011745.1:g.48370T>A , LRG_1022:g.48370T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227-14T>A MANE Select ENSP00000256958.2:n.227-14T>A
ENST00000256958.2:c.227-14T>A ENSP00000256958.2:n.227-14T>A
ENST00000543498.5:c.426-2213T>A
NM_006446.4:c.227-14T>A , LRG_1022t1:c.227-14T>A NP_006437.3:n.227-14T>A
NM_006446.5:c.227-14T>A MANE Select NP_006437.3:n.227-14T>A
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