Canonical Allele Identifier: CA609999849

Gene: OLFM4

Linked Data

• dbSNP Id: rs1053105891
• gnomAD v2: 13-53625716-A-T
• gnomAD v3: 13-53051581-A-T
• gnomAD v4: 13-53051581-A-T
• MyVariant Identifiers: chr13:g.53625716A>T (hg19) ; chr13:g.53051581A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.53051581A>T , CM000675.2:g.53051581A>T	GRCh38
NC_000013.10:g.53625716A>T , CM000675.1:g.53625716A>T	GRCh37
NC_000013.9:g.52523717A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219022.3:c.*810A>T MANE Select	ENSP00000219022.2:n.*810A>T
ENST00000219022.2:c.*810A>T	ENSP00000219022.2:n.*810A>T
NM_006418.4:c.*810A>T	NP_006409.3:n.*810A>T
NM_006418.5:c.*810A>T MANE Select	NP_006409.3:n.*810A>T