Canonical Allele Identifier: CA1589086793
Gene: POU4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340132T= , CM000667.2:g.146340132T= GRCh38
NC_000005.9:g.145719695T= , CM000667.1:g.145719695T= GRCh37
NC_000005.8:g.145699888T= NCBI36
NG_011885.1:g.6109T=

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.705T= MANE Select ENSP00000495718.1:p.Thr235=
ENST00000230732.4:c.705T= ENSP00000230732.4:p.Thr235=
NM_002700.2:c.705T= NP_002691.1:p.Thr235=
NM_002700.3:c.705T= MANE Select NP_002691.1:p.Thr235=