Canonical Allele Identifier: CA250176552
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs532362371
gnomAD v3: 13-53051576-A-T
gnomAD v4: 13-53051576-A-T
MyVariant Identifiers: chr13:g.53625711A>T (hg19) chr13:g.53051576A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051576A>T , CM000675.2:g.53051576A>T GRCh38
NC_000013.10:g.53625711A>T , CM000675.1:g.53625711A>T GRCh37
NC_000013.9:g.52523712A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*805A>T MANE Select ENSP00000219022.2:n.*805A>T
ENST00000219022.2:c.*805A>T ENSP00000219022.2:n.*805A>T
NM_006418.4:c.*805A>T NP_006409.3:n.*805A>T
NM_006418.5:c.*805A>T MANE Select NP_006409.3:n.*805A>T
Search 100 bp 5'
Search 100 bp 3'