Canonical Allele Identifier: CA1589086702
Gene: POU4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339948C= , CM000667.2:g.146339948C= GRCh38
NC_000005.9:g.145719511C= , CM000667.1:g.145719511C= GRCh37
NC_000005.8:g.145699704C= NCBI36
NG_011885.1:g.5925C=

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.521C= MANE Select ENSP00000495718.1:p.Pro174=
ENST00000230732.4:c.521C= ENSP00000230732.4:p.Pro174=
NM_002700.2:c.521C= NP_002691.1:p.Pro174=
NM_002700.3:c.521C= MANE Select NP_002691.1:p.Pro174=