Canonical Allele Identifier: CA384104381
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174700T>A , CM000674.2:g.21174700T>A GRCh38
NC_000012.11:g.21327634T>A , CM000674.1:g.21327634T>A GRCh37
NC_000012.10:g.21218901T>A NCBI36
NG_011745.1:g.48507T>A , LRG_1022:g.48507T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256958.3:c.350T>A MANE Select ENSP00000256958.2:p.Phe117Tyr
ENST00000256958.2:c.350T>A ENSP00000256958.2:p.Phe117Tyr
ENST00000543498.5:c.426-2076T>A
NM_006446.4:c.350T>A , LRG_1022t1:c.350T>A NP_006437.3:p.Phe117Tyr
NM_006446.5:c.350T>A MANE Select NP_006437.3:p.Phe117Tyr