Canonical Allele Identifier: CA413751859
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763921T>A (hg19) chrX:g.83508913T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508913T>A , CM000685.2:g.83508913T>A GRCh38
NC_000023.10:g.82763921T>A , CM000685.1:g.82763921T>A GRCh37
NC_000023.9:g.82650577T>A NCBI36
NG_009936.2:g.5653T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.589T>A MANE Select ENSP00000495996.1:p.Phe197Ile
ENST00000373200.4:c.589T>A ENSP00000362296.2:p.Phe197Ile
NM_000307.4:c.589T>A NP_000298.3:p.Phe197Ile
NM_000307.5:c.589T>A MANE Select NP_000298.3:p.Phe197Ile
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