Canonical Allele Identifier: CA517478824
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763324T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508316T>C , CM000685.2:g.83508316T>C GRCh38
NC_000023.10:g.82763324T>C , CM000685.1:g.82763324T>C GRCh37
NC_000023.9:g.82649980T>C NCBI36
NG_009936.2:g.5056T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.-9T>C MANE Select ENSP00000495996.1:n.-9T>C
ENST00000373200.4:c.-9T>C ENSP00000362296.2:n.-9T>C
NM_000307.4:c.-9T>C NP_000298.3:n.-9T>C
NM_000307.5:c.-9T>C MANE Select NP_000298.3:n.-9T>C