Canonical Allele Identifier: CA250176512
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs956159114
gnomAD v3: 13-53051543-AC-A
gnomAD v4: 13-53051543-AC-A
MyVariant Identifiers: chr13:g.53625679del (hg19) chr13:g.53051544del (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*778del MANE Select ENSP00000219022.2:n.*778del
ENST00000219022.2:c.*778del ENSP00000219022.2:n.*778del
NM_006418.4:c.*778del NP_006409.3:n.*778del
NM_006418.5:c.*778del MANE Select NP_006409.3:n.*778del
Search 100 bp 5'
Search 100 bp 3'