Canonical Allele Identifier: CA1589086776
Gene: POU4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340090C= , CM000667.2:g.146340090C= GRCh38
NC_000005.9:g.145719653C= , CM000667.1:g.145719653C= GRCh37
NC_000005.8:g.145699846C= NCBI36
NG_011885.1:g.6067C=

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.663C= MANE Select ENSP00000495718.1:p.Gly221=
ENST00000230732.4:c.663C= ENSP00000230732.4:p.Gly221=
NM_002700.2:c.663C= NP_002691.1:p.Gly221=
NM_002700.3:c.663C= MANE Select NP_002691.1:p.Gly221=