Canonical Allele Identifier: CA517478852
Gene: POU3F4 HGNC NCBI

Linked Data

gnomAD v4: X-83508321-G-T
MyVariant Identifiers: chrX:g.82763329G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508321G>T , CM000685.2:g.83508321G>T GRCh38
NC_000023.10:g.82763329G>T , CM000685.1:g.82763329G>T GRCh37
NC_000023.9:g.82649985G>T NCBI36
NG_009936.2:g.5061G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.-4G>T MANE Select ENSP00000495996.1:n.-4G>T
ENST00000373200.4:c.-4G>T ENSP00000362296.2:n.-4G>T
NM_000307.4:c.-4G>T NP_000298.3:n.-4G>T
NM_000307.5:c.-4G>T MANE Select NP_000298.3:n.-4G>T
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