Canonical Allele Identifier: CA699054003
Gene: OLFM4 HGNC NCBI

Linked Data

dbSNP Id: rs1218796065
gnomAD v4: 13-53051758-G-T
MyVariant Identifiers: chr13:g.53625893G>T (hg19) chr13:g.53051758G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.53051758G>T , CM000675.2:g.53051758G>T GRCh38
NC_000013.10:g.53625893G>T , CM000675.1:g.53625893G>T GRCh37
NC_000013.9:g.52523894G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219022.3:c.*987G>T MANE Select ENSP00000219022.2:n.*987G>T
ENST00000219022.2:c.*987G>T ENSP00000219022.2:n.*987G>T
NM_006418.4:c.*987G>T NP_006409.3:n.*987G>T
NM_006418.5:c.*987G>T MANE Select NP_006409.3:n.*987G>T
Search 100 bp 5'
Search 100 bp 3'