Canonical Allele Identifier: CA699053927
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1438274395
gnomAD v3: 13-53051584-T-G
gnomAD v4: 13-53051584-T-G
MyVariant Identifiers: chr13:g.53625719T>G (hg19) chr13:g.53051584T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051584T>G , CM000675.2:g.53051584T>G GRCh38
NC_000013.10:g.53625719T>G , CM000675.1:g.53625719T>G GRCh37
NC_000013.9:g.52523720T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*813T>G MANE Select ENSP00000219022.2:n.*813T>G
ENST00000219022.2:c.*813T>G ENSP00000219022.2:n.*813T>G
NM_006418.4:c.*813T>G NP_006409.3:n.*813T>G
NM_006418.5:c.*813T>G MANE Select NP_006409.3:n.*813T>G
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