Canonical Allele Identifier: CA517478580
Gene: POU3F4 HGNC NCBI

Linked Data

gnomAD v4: X-83508272-G-T
MyVariant Identifiers: chrX:g.82763280G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508272G>T , CM000685.2:g.83508272G>T GRCh38
NC_000023.10:g.82763280G>T , CM000685.1:g.82763280G>T GRCh37
NC_000023.9:g.82649936G>T NCBI36
NG_009936.2:g.5012G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-53G>T ENSP00000362296.2:n.-53G>T
NM_000307.4:c.-53G>T NP_000298.3:n.-53G>T