Canonical Allele Identifier: CA10462742
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs767261687
gnomAD v2: X-82763487-C-A
gnomAD v3: X-83508479-C-A
gnomAD v4: X-83508479-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508479C>A , CM000685.2:g.83508479C>A GRCh38
NC_000023.10:g.82763487C>A , CM000685.1:g.82763487C>A GRCh37
NC_000023.9:g.82650143C>A NCBI36
NG_009936.2:g.5219C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.155C>A MANE Select ENSP00000495996.1:p.Pro52His
ENST00000373200.4:c.155C>A ENSP00000362296.2:p.Pro52His
NM_000307.4:c.155C>A NP_000298.3:p.Pro52His
NM_000307.5:c.155C>A MANE Select NP_000298.3:p.Pro52His