Canonical Allele Identifier: CA517478579
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763280G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508272G>C , CM000685.2:g.83508272G>C GRCh38
NC_000023.10:g.82763280G>C , CM000685.1:g.82763280G>C GRCh37
NC_000023.9:g.82649936G>C NCBI36
NG_009936.2:g.5012G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-53G>C ENSP00000362296.2:n.-53G>C
NM_000307.4:c.-53G>C NP_000298.3:n.-53G>C