Canonical Allele Identifier: CA250176577

Gene: OLFM4

Linked Data

• dbSNP Id: rs751703269
• MyVariant Identifiers: chr13:g.53625774C>A (hg19) ; chr13:g.53051639C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.53051639C>A , CM000675.2:g.53051639C>A	GRCh38
NC_000013.10:g.53625774C>A , CM000675.1:g.53625774C>A	GRCh37
NC_000013.9:g.52523775C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219022.3:c.*868C>A MANE Select	ENSP00000219022.2:n.*868C>A
ENST00000219022.2:c.*868C>A	ENSP00000219022.2:n.*868C>A
NM_006418.4:c.*868C>A	NP_006409.3:n.*868C>A
NM_006418.5:c.*868C>A MANE Select	NP_006409.3:n.*868C>A