Canonical Allele Identifier: CA413752027
Gene: POU3F4 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.662C>T MANE Select ENSP00000495996.1:p.Thr221Ile
ENST00000373200.4:c.662C>T ENSP00000362296.2:p.Thr221Ile
NM_000307.4:c.662C>T NP_000298.3:p.Thr221Ile
NM_000307.5:c.662C>T MANE Select NP_000298.3:p.Thr221Ile
Search 100 bp 5'
Search 100 bp 3'