Canonical Allele Identifier: CA384105522
Gene: SLCO1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21178624G>T , CM000674.2:g.21178624G>T GRCh38
NC_000012.11:g.21331558G>T , CM000674.1:g.21331558G>T GRCh37
NC_000012.10:g.21222825G>T NCBI36
NG_011745.1:g.52431G>T , LRG_1022:g.52431G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.530G>T MANE Select ENSP00000256958.2:p.Gly177Val
ENST00000256958.2:c.530G>T ENSP00000256958.2:p.Gly177Val
NM_006446.4:c.530G>T , LRG_1022t1:c.530G>T NP_006437.3:p.Gly177Val
NM_006446.5:c.530G>T MANE Select NP_006437.3:p.Gly177Val