Canonical Allele Identifier: CA2092048038
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1826570712
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051573T>A , CM000675.2:g.53051573T>A GRCh38
NC_000013.10:g.53625708T>A , CM000675.1:g.53625708T>A GRCh37
NC_000013.9:g.52523709T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*802T>A MANE Select ENSP00000219022.2:n.*802T>A
ENST00000219022.2:c.*802T>A ENSP00000219022.2:n.*802T>A
NM_006418.4:c.*802T>A NP_006409.3:n.*802T>A
NM_006418.5:c.*802T>A MANE Select NP_006409.3:n.*802T>A
Search 100 bp 5'
Search 100 bp 3'