Canonical Allele Identifier: CA413751182
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1424403763
gnomAD v2: X-82763607-C-A
gnomAD v4: X-83508599-C-A
MyVariant Identifiers: chrX:g.82763607C>A (hg19) chrX:g.83508599C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508599C>A , CM000685.2:g.83508599C>A GRCh38
NC_000023.10:g.82763607C>A , CM000685.1:g.82763607C>A GRCh37
NC_000023.9:g.82650263C>A NCBI36
NG_009936.2:g.5339C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.275C>A MANE Select ENSP00000495996.1:p.Ala92Glu
ENST00000373200.4:c.275C>A ENSP00000362296.2:p.Ala92Glu
NM_000307.4:c.275C>A NP_000298.3:p.Ala92Glu
NM_000307.5:c.275C>A MANE Select NP_000298.3:p.Ala92Glu
Search 100 bp 5'
Search 100 bp 3'