Canonical Allele Identifier: CA517479355
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763944A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508936A>G , CM000685.2:g.83508936A>G GRCh38
NC_000023.10:g.82763944A>G , CM000685.1:g.82763944A>G GRCh37
NC_000023.9:g.82650600A>G NCBI36
NG_009936.2:g.5676A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.612A>G MANE Select ENSP00000495996.1:p.Arg204=
ENST00000373200.4:c.612A>G ENSP00000362296.2:p.Arg204=
NM_000307.4:c.612A>G NP_000298.3:p.Arg204=
NM_000307.5:c.612A>G MANE Select NP_000298.3:p.Arg204=