Canonical Allele Identifier: CA517478541
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763271A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508263A>T , CM000685.2:g.83508263A>T GRCh38
NC_000023.10:g.82763271A>T , CM000685.1:g.82763271A>T GRCh37
NC_000023.9:g.82649927A>T NCBI36
NG_009936.2:g.5003A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-62A>T ENSP00000362296.2:n.-62A>T
NM_000307.4:c.-62A>T NP_000298.3:n.-62A>T