Canonical Allele Identifier: CA1589086857
Gene: POU4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340263C= , CM000667.2:g.146340263C= GRCh38
NC_000005.9:g.145719826C= , CM000667.1:g.145719826C= GRCh37
NC_000005.8:g.145700019C= NCBI36
NG_011885.1:g.6240C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.836C= MANE Select ENSP00000495718.1:p.Thr279=
ENST00000230732.4:c.836C= ENSP00000230732.4:p.Thr279=
NM_002700.2:c.836C= NP_002691.1:p.Thr279=
NM_002700.3:c.836C= MANE Select NP_002691.1:p.Thr279=