Canonical Allele Identifier: CA413752029
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763994C>A (hg19) chrX:g.83508986C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508986C>A , CM000685.2:g.83508986C>A GRCh38
NC_000023.10:g.82763994C>A , CM000685.1:g.82763994C>A GRCh37
NC_000023.9:g.82650650C>A NCBI36
NG_009936.2:g.5726C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.662C>A MANE Select ENSP00000495996.1:p.Thr221Lys
ENST00000373200.4:c.662C>A ENSP00000362296.2:p.Thr221Lys
NM_000307.4:c.662C>A NP_000298.3:p.Thr221Lys
NM_000307.5:c.662C>A MANE Select NP_000298.3:p.Thr221Lys
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