Canonical Allele Identifier: CA699053904
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1169954670
gnomAD v4: 13-53051561-T-C
MyVariant Identifiers: chr13:g.53625696T>C (hg19) chr13:g.53051561T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051561T>C , CM000675.2:g.53051561T>C GRCh38
NC_000013.10:g.53625696T>C , CM000675.1:g.53625696T>C GRCh37
NC_000013.9:g.52523697T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*790T>C MANE Select ENSP00000219022.2:n.*790T>C
ENST00000219022.2:c.*790T>C ENSP00000219022.2:n.*790T>C
NM_006418.4:c.*790T>C NP_006409.3:n.*790T>C
NM_006418.5:c.*790T>C MANE Select NP_006409.3:n.*790T>C
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