Canonical Allele Identifier: CA517478502
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763262G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508254G>C , CM000685.2:g.83508254G>C GRCh38
NC_000023.10:g.82763262G>C , CM000685.1:g.82763262G>C GRCh37
NC_000023.9:g.82649918G>C NCBI36
NG_009936.2:g.4994G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-71G>C ENSP00000362296.2:n.-71G>C