Canonical Allele Identifier: CA517479445
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82764193G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83509185G>T , CM000685.2:g.83509185G>T GRCh38
NC_000023.10:g.82764193G>T , CM000685.1:g.82764193G>T GRCh37
NC_000023.9:g.82650849G>T NCBI36
NG_009936.2:g.5925G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.861G>T MANE Select ENSP00000495996.1:p.Val287=
ENST00000373200.4:c.861G>T ENSP00000362296.2:p.Val287=
NM_000307.4:c.861G>T NP_000298.3:p.Val287=
NM_000307.5:c.861G>T MANE Select NP_000298.3:p.Val287=
Search 100 bp 5'
Search 100 bp 3'