Canonical Allele Identifier: CA517478601
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763285A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508277A>G , CM000685.2:g.83508277A>G GRCh38
NC_000023.10:g.82763285A>G , CM000685.1:g.82763285A>G GRCh37
NC_000023.9:g.82649941A>G NCBI36
NG_009936.2:g.5017A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-48A>G ENSP00000362296.2:n.-48A>G
NM_000307.4:c.-48A>G NP_000298.3:n.-48A>G
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