Canonical Allele Identifier: CA255984
Gene: POU3F4 HGNC NCBI

Linked Data

ClinVar Variation Id: 11684
ClinVar RCV Id: RCV000012450
dbSNP Id: rs104894924
MyVariant Identifiers: chrX:g.82764299C>G (hg19) chrX:g.83509291C>G (hg38)
PubMed: PMID:9298820
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83509291C>G , CM000685.2:g.83509291C>G GRCh38
NC_000023.10:g.82764299C>G , CM000685.1:g.82764299C>G GRCh37
NC_000023.9:g.82650955C>G NCBI36
NG_009936.2:g.6031C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.967C>G MANE Select ENSP00000495996.1:p.Arg323Gly
ENST00000373200.4:c.967C>G ENSP00000362296.2:p.Arg323Gly
NM_000307.4:c.967C>G NP_000298.3:p.Arg323Gly
NM_000307.5:c.967C>G MANE Select NP_000298.3:p.Arg323Gly
Search 100 bp 5'
Search 100 bp 3'