Canonical Allele Identifier: CA2092048035
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1593484543
gnomAD v4: 13-53051571-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051571A>G , CM000675.2:g.53051571A>G GRCh38
NC_000013.10:g.53625706A>G , CM000675.1:g.53625706A>G GRCh37
NC_000013.9:g.52523707A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*800A>G MANE Select ENSP00000219022.2:n.*800A>G
ENST00000219022.2:c.*800A>G ENSP00000219022.2:n.*800A>G
NM_006418.4:c.*800A>G NP_006409.3:n.*800A>G
NM_006418.5:c.*800A>G MANE Select NP_006409.3:n.*800A>G
Search 100 bp 5'
Search 100 bp 3'