Canonical Allele Identifier: CA2092048114
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1954750363
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051753T>C , CM000675.2:g.53051753T>C GRCh38
NC_000013.10:g.53625888T>C , CM000675.1:g.53625888T>C GRCh37
NC_000013.9:g.52523889T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219022.3:c.*982T>C MANE Select ENSP00000219022.2:n.*982T>C
ENST00000219022.2:c.*982T>C ENSP00000219022.2:n.*982T>C
NM_006418.4:c.*982T>C NP_006409.3:n.*982T>C
NM_006418.5:c.*982T>C MANE Select NP_006409.3:n.*982T>C
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