Canonical Allele Identifier: CA6476725
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs755871104

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.530del MANE Select ENSP00000256958.2:p.Gly177ValfsTer7
ENST00000256958.2:c.530del ENSP00000256958.2:p.Gly177ValfsTer7
NM_006446.4:c.530del , LRG_1022t1:c.530del NP_006437.3:p.Gly177ValfsTer7
NM_006446.5:c.530del MANE Select NP_006437.3:p.Gly177ValfsTer7