Canonical Allele Identifier: CA233559655
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs56061388

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174595T>C , CM000674.2:g.21174595T>C GRCh38
NC_000012.11:g.21327529T>C , CM000674.1:g.21327529T>C GRCh37
NC_000012.10:g.21218796T>C NCBI36
NG_011745.1:g.48402T>C , LRG_1022:g.48402T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.245T>C MANE Select ENSP00000256958.2:p.Val82Ala
ENST00000256958.2:c.245T>C ENSP00000256958.2:p.Val82Ala
ENST00000543498.5:n.426-2181T>C
NM_006446.4:c.245T>C , LRG_1022t1:c.245T>C NP_006437.3:p.Val82Ala
NM_006446.5:c.245T>C MANE Select NP_006437.3:p.Val82Ala