Canonical Allele Identifier: CA10623123
Gene: POU4F3 HGNC NCBI

Linked Data

ClinVar Variation Id: 351382
ClinVar RCV Id: RCV000380789
dbSNP Id: rs886060063

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340004C>T , CM000667.2:g.146340004C>T GRCh38
NC_000005.9:g.145719567C>T , CM000667.1:g.145719567C>T GRCh37
NC_000005.8:g.145699760C>T NCBI36
NG_011885.1:g.5981C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.577C>T MANE Select ENSP00000495718.1:p.Arg193Cys
ENST00000230732.4:c.577C>T ENSP00000230732.4:p.Arg193Cys
NM_002700.2:c.577C>T NP_002691.1:p.Arg193Cys
NM_002700.3:c.577C>T MANE Select NP_002691.1:p.Arg193Cys