Canonical Allele Identifier: CA10462783
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs765569063
ExAC: X:82763811 A / G
gnomAD v2: X-82763811-A-G
gnomAD v3: X-83508803-A-G
gnomAD v4: X-83508803-A-G
MyVariant Identifiers: chrX:g.82763811A>G (hg19) chrX:g.83508803A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508803A>G , CM000685.2:g.83508803A>G GRCh38
NC_000023.10:g.82763811A>G , CM000685.1:g.82763811A>G GRCh37
NC_000023.9:g.82650467A>G NCBI36
NG_009936.2:g.5543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.479A>G MANE Select ENSP00000495996.1:p.Gln160Arg
ENST00000373200.4:c.479A>G ENSP00000362296.2:p.Gln160Arg
NM_000307.4:c.479A>G NP_000298.3:p.Gln160Arg
NM_000307.5:c.479A>G MANE Select NP_000298.3:p.Gln160Arg
Search 100 bp 5'
Search 100 bp 3'