Canonical Allele Identifier: CA250176601
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1004793713
gnomAD v3: 13-53051733-T-A
gnomAD v4: 13-53051733-T-A
MyVariant Identifiers: chr13:g.53625868T>A (hg19) chr13:g.53051733T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051733T>A , CM000675.2:g.53051733T>A GRCh38
NC_000013.10:g.53625868T>A , CM000675.1:g.53625868T>A GRCh37
NC_000013.9:g.52523869T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*962T>A MANE Select ENSP00000219022.2:n.*962T>A
ENST00000219022.2:c.*962T>A ENSP00000219022.2:n.*962T>A
NM_006418.4:c.*962T>A NP_006409.3:n.*962T>A
NM_006418.5:c.*962T>A MANE Select NP_006409.3:n.*962T>A
Search 100 bp 5'
Search 100 bp 3'