Canonical Allele Identifier: CA2092048108
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1954750305
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051739A>G , CM000675.2:g.53051739A>G GRCh38
NC_000013.10:g.53625874A>G , CM000675.1:g.53625874A>G GRCh37
NC_000013.9:g.52523875A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*968A>G MANE Select ENSP00000219022.2:n.*968A>G
ENST00000219022.2:c.*968A>G ENSP00000219022.2:n.*968A>G
NM_006418.4:c.*968A>G NP_006409.3:n.*968A>G
NM_006418.5:c.*968A>G MANE Select NP_006409.3:n.*968A>G
Search 100 bp 5'
Search 100 bp 3'