Canonical Allele Identifier: CA1589086802
Gene: POU4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340151A= , CM000667.2:g.146340151A= GRCh38
NC_000005.9:g.145719714A= , CM000667.1:g.145719714A= GRCh37
NC_000005.8:g.145699907A= NCBI36
NG_011885.1:g.6128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.724A= MANE Select ENSP00000495718.1:p.Ile242=
ENST00000230732.4:c.724A= ENSP00000230732.4:p.Ile242=
NM_002700.2:c.724A= NP_002691.1:p.Ile242=
NM_002700.3:c.724A= MANE Select NP_002691.1:p.Ile242=