Canonical Allele Identifier: CA517445854
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82764286G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83509278G>A , CM000685.2:g.83509278G>A GRCh38
NC_000023.10:g.82764286G>A , CM000685.1:g.82764286G>A GRCh37
NC_000023.9:g.82650942G>A NCBI36
NG_009936.2:g.6018G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.954G>A MANE Select ENSP00000495996.1:p.Glu318=
ENST00000373200.4:c.954G>A ENSP00000362296.2:p.Glu318=
NM_000307.4:c.954G>A NP_000298.3:p.Glu318=
NM_000307.5:c.954G>A MANE Select NP_000298.3:p.Glu318=