Canonical Allele Identifier: CA413750913
Gene: POU3F4 HGNC NCBI

Linked Data

gnomAD v4: X-83508473-G-T
MyVariant Identifiers: chrX:g.82763481G>T (hg19) chrX:g.83508473G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508473G>T , CM000685.2:g.83508473G>T GRCh38
NC_000023.10:g.82763481G>T , CM000685.1:g.82763481G>T GRCh37
NC_000023.9:g.82650137G>T NCBI36
NG_009936.2:g.5213G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.149G>T MANE Select ENSP00000495996.1:p.Gly50Val
ENST00000373200.4:c.149G>T ENSP00000362296.2:p.Gly50Val
NM_000307.4:c.149G>T NP_000298.3:p.Gly50Val
NM_000307.5:c.149G>T MANE Select NP_000298.3:p.Gly50Val
Search 100 bp 5'
Search 100 bp 3'