Canonical Allele Identifier: CA699053938
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1317064307
gnomAD v3: 13-53051594-C-T
gnomAD v4: 13-53051594-C-T
MyVariant Identifiers: chr13:g.53625729C>T (hg19) chr13:g.53051594C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051594C>T , CM000675.2:g.53051594C>T GRCh38
NC_000013.10:g.53625729C>T , CM000675.1:g.53625729C>T GRCh37
NC_000013.9:g.52523730C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*823C>T MANE Select ENSP00000219022.2:n.*823C>T
ENST00000219022.2:c.*823C>T ENSP00000219022.2:n.*823C>T
NM_006418.4:c.*823C>T NP_006409.3:n.*823C>T
NM_006418.5:c.*823C>T MANE Select NP_006409.3:n.*823C>T
Search 100 bp 5'
Search 100 bp 3'