Canonical Allele Identifier: CA609999847
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs956159114

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051549dup , CM000675.2:g.53051549dup GRCh38
NC_000013.10:g.53625684dup , CM000675.1:g.53625684dup GRCh37
NC_000013.9:g.52523685dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*778dup MANE Select ENSP00000219022.2:n.*778dup
ENST00000219022.2:c.*778dup ENSP00000219022.2:n.*778dup
NM_006418.4:c.*778dup NP_006409.3:n.*778dup
NM_006418.5:c.*778dup MANE Select NP_006409.3:n.*778dup