Canonical Allele Identifier: CA3491113
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs759912218

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339773G>A , CM000667.2:g.146339773G>A GRCh38
NC_000005.9:g.145719336G>A , CM000667.1:g.145719336G>A GRCh37
NC_000005.8:g.145699529G>A NCBI36
NG_011885.1:g.5750G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.346G>A MANE Select ENSP00000495718.1:p.Glu116Lys
ENST00000230732.4:c.346G>A ENSP00000230732.4:p.Glu116Lys
NM_002700.2:c.346G>A NP_002691.1:p.Glu116Lys
NM_002700.3:c.346G>A MANE Select NP_002691.1:p.Glu116Lys