Canonical Allele Identifier: CA517478603
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1186537483
gnomAD v2: X-82763286-G-T
MyVariant Identifiers: chrX:g.82763286G>T (hg19) chrX:g.83508278G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508278G>T , CM000685.2:g.83508278G>T GRCh38
NC_000023.10:g.82763286G>T , CM000685.1:g.82763286G>T GRCh37
NC_000023.9:g.82649942G>T NCBI36
NG_009936.2:g.5018G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-47G>T ENSP00000362296.2:n.-47G>T
NM_000307.4:c.-47G>T NP_000298.3:n.-47G>T
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