Canonical Allele Identifier: CA517478631
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763291T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508283T>G , CM000685.2:g.83508283T>G GRCh38
NC_000023.10:g.82763291T>G , CM000685.1:g.82763291T>G GRCh37
NC_000023.9:g.82649947T>G NCBI36
NG_009936.2:g.5023T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-42T>G ENSP00000362296.2:n.-42T>G
NM_000307.4:c.-42T>G NP_000298.3:n.-42T>G
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