Canonical Allele Identifier: CA517478620
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763289G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508281G>C , CM000685.2:g.83508281G>C GRCh38
NC_000023.10:g.82763289G>C , CM000685.1:g.82763289G>C GRCh37
NC_000023.9:g.82649945G>C NCBI36
NG_009936.2:g.5021G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-44G>C ENSP00000362296.2:n.-44G>C
NM_000307.4:c.-44G>C NP_000298.3:n.-44G>C
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