Canonical Allele Identifier: CA699053913
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs947143325
gnomAD v3: 13-53051567-G-C
gnomAD v4: 13-53051567-G-C
MyVariant Identifiers: chr13:g.53625702G>C (hg19) chr13:g.53051567G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051567G>C , CM000675.2:g.53051567G>C GRCh38
NC_000013.10:g.53625702G>C , CM000675.1:g.53625702G>C GRCh37
NC_000013.9:g.52523703G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*796G>C MANE Select ENSP00000219022.2:n.*796G>C
ENST00000219022.2:c.*796G>C ENSP00000219022.2:n.*796G>C
NM_006418.4:c.*796G>C NP_006409.3:n.*796G>C
NM_006418.5:c.*796G>C MANE Select NP_006409.3:n.*796G>C
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