Canonical Allele Identifier: CA517479000
Gene: POU3F4 HGNC NCBI

Linked Data

gnomAD v4: X-83508819-G-A
MyVariant Identifiers: chrX:g.82763827G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508819G>A , CM000685.2:g.83508819G>A GRCh38
NC_000023.10:g.82763827G>A , CM000685.1:g.82763827G>A GRCh37
NC_000023.9:g.82650483G>A NCBI36
NG_009936.2:g.5559G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.495G>A MANE Select ENSP00000495996.1:p.Val165=
ENST00000373200.4:c.495G>A ENSP00000362296.2:p.Val165=
NM_000307.4:c.495G>A NP_000298.3:p.Val165=
NM_000307.5:c.495G>A MANE Select NP_000298.3:p.Val165=
Search 100 bp 5'
Search 100 bp 3'