Canonical Allele Identifier: CA3491147
Gene: POU4F3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372853
ClinVar RCV Id: RCV000413888

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339929del , CM000667.2:g.146339929del GRCh38
NC_000005.8:g.145699685del NCBI36
NC_000005.9:g.145719492del , CM000667.1:g.145719492del GRCh37
NG_011885.1:g.5906del

Transcript Alleles

HGVS Amino-acid change
ENST00000230732.4:c.502del ENSP00000230732.4:p.Ala168ProfsTer?
NM_002700.2:c.502del NP_002691.1:p.Ala168ProfsTer?