Canonical Allele Identifier: CA128861198
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs924797665

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340189G>T , CM000667.2:g.146340189G>T GRCh38
NC_000005.9:g.145719752G>T , CM000667.1:g.145719752G>T GRCh37
NC_000005.8:g.145699945G>T NCBI36
NG_011885.1:g.6166G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.762G>T MANE Select ENSP00000495718.1:p.Glu254Asp
ENST00000230732.4:c.762G>T ENSP00000230732.4:p.Glu254Asp
NM_002700.2:c.762G>T NP_002691.1:p.Glu254Asp
NM_002700.3:c.762G>T MANE Select NP_002691.1:p.Glu254Asp