Canonical Allele Identifier: CA255977
Gene: POU3F4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11680
ClinVar RCV Id: RCV000012446
dbSNP Id: rs104894922

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83509324A>G , CM000685.2:g.83509324A>G GRCh38
NC_000023.10:g.82764332A>G , CM000685.1:g.82764332A>G GRCh37
NC_000023.9:g.82650988A>G NCBI36
NG_009936.2:g.6064A>G

Transcript Alleles

HGVS Amino-acid change
NM_000307.4:c.1000A>G VV NP_000298.3:p.Lys334Glu
ENST00000373200.4:c.1000A>G ENSP00000362296.2:p.Lys334Glu