Canonical Allele Identifier: CA413752028
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763994C>G (hg19) chrX:g.83508986C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508986C>G , CM000685.2:g.83508986C>G GRCh38
NC_000023.10:g.82763994C>G , CM000685.1:g.82763994C>G GRCh37
NC_000023.9:g.82650650C>G NCBI36
NG_009936.2:g.5726C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.662C>G MANE Select ENSP00000495996.1:p.Thr221Arg
ENST00000373200.4:c.662C>G ENSP00000362296.2:p.Thr221Arg
NM_000307.4:c.662C>G NP_000298.3:p.Thr221Arg
NM_000307.5:c.662C>G MANE Select NP_000298.3:p.Thr221Arg
Search 100 bp 5'
Search 100 bp 3'