Canonical Allele Identifier: CA2092048047
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1954748734
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051586A>G , CM000675.2:g.53051586A>G GRCh38
NC_000013.10:g.53625721A>G , CM000675.1:g.53625721A>G GRCh37
NC_000013.9:g.52523722A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*815A>G MANE Select ENSP00000219022.2:n.*815A>G
ENST00000219022.2:c.*815A>G ENSP00000219022.2:n.*815A>G
NM_006418.4:c.*815A>G NP_006409.3:n.*815A>G
NM_006418.5:c.*815A>G MANE Select NP_006409.3:n.*815A>G
Search 100 bp 5'
Search 100 bp 3'