Canonical Allele Identifier: CA699053987
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1234597150
gnomAD v3: 13-53051706-G-A
gnomAD v4: 13-53051706-G-A
MyVariant Identifiers: chr13:g.53625841G>A (hg19) chr13:g.53051706G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051706G>A , CM000675.2:g.53051706G>A GRCh38
NC_000013.10:g.53625841G>A , CM000675.1:g.53625841G>A GRCh37
NC_000013.9:g.52523842G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*935G>A MANE Select ENSP00000219022.2:n.*935G>A
ENST00000219022.2:c.*935G>A ENSP00000219022.2:n.*935G>A
NM_006418.4:c.*935G>A NP_006409.3:n.*935G>A
NM_006418.5:c.*935G>A MANE Select NP_006409.3:n.*935G>A
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