Canonical Allele Identifier: CA250176548
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs529149404
gnomAD v4: 13-53051568-C-A
MyVariant Identifiers: chr13:g.53625703C>A (hg19) chr13:g.53051568C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051568C>A , CM000675.2:g.53051568C>A GRCh38
NC_000013.10:g.53625703C>A , CM000675.1:g.53625703C>A GRCh37
NC_000013.9:g.52523704C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*797C>A MANE Select ENSP00000219022.2:n.*797C>A
ENST00000219022.2:c.*797C>A ENSP00000219022.2:n.*797C>A
NM_006418.4:c.*797C>A NP_006409.3:n.*797C>A
NM_006418.5:c.*797C>A MANE Select NP_006409.3:n.*797C>A
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