Canonical Allele Identifier: CA517478789
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1433636877
MyVariant Identifiers: chrX:g.82763318G>A (hg19) chrX:g.83508310G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508310G>A , CM000685.2:g.83508310G>A GRCh38
NC_000023.10:g.82763318G>A , CM000685.1:g.82763318G>A GRCh37
NC_000023.9:g.82649974G>A NCBI36
NG_009936.2:g.5050G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.-15G>A MANE Select ENSP00000495996.1:n.-15G>A
ENST00000373200.4:c.-15G>A ENSP00000362296.2:n.-15G>A
NM_000307.4:c.-15G>A NP_000298.3:n.-15G>A
NM_000307.5:c.-15G>A MANE Select NP_000298.3:n.-15G>A
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