Canonical Allele Identifier: CA1589086598
Gene: POU4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339760G= , CM000667.2:g.146339760G= GRCh38
NC_000005.9:g.145719323G= , CM000667.1:g.145719323G= GRCh37
NC_000005.8:g.145699516G= NCBI36
NG_011885.1:g.5737G=

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.333G= MANE Select ENSP00000495718.1:p.Val111=
ENST00000230732.4:c.333G= ENSP00000230732.4:p.Val111=
NM_002700.2:c.333G= NP_002691.1:p.Val111=
NM_002700.3:c.333G= MANE Select NP_002691.1:p.Val111=