Canonical Allele Identifier: CA517478662
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763989G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508981G>T , CM000685.2:g.83508981G>T GRCh38
NC_000023.10:g.82763989G>T , CM000685.1:g.82763989G>T GRCh37
NC_000023.9:g.82650645G>T NCBI36
NG_009936.2:g.5721G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.657G>T MANE Select ENSP00000495996.1:p.Leu219=
ENST00000373200.4:c.657G>T ENSP00000362296.2:p.Leu219=
NM_000307.4:c.657G>T NP_000298.3:p.Leu219=
NM_000307.5:c.657G>T MANE Select NP_000298.3:p.Leu219=
Search 100 bp 5'
Search 100 bp 3'