Canonical Allele Identifier: CA413750675
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1925823915
gnomAD v3: X-83508367-A-C
gnomAD v4: X-83508367-A-C
MyVariant Identifiers: chrX:g.82763375A>C (hg19) chrX:g.83508367A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508367A>C , CM000685.2:g.83508367A>C GRCh38
NC_000023.10:g.82763375A>C , CM000685.1:g.82763375A>C GRCh37
NC_000023.9:g.82650031A>C NCBI36
NG_009936.2:g.5107A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.43A>C MANE Select ENSP00000495996.1:p.Thr15Pro
ENST00000373200.4:c.43A>C ENSP00000362296.2:p.Thr15Pro
NM_000307.4:c.43A>C NP_000298.3:p.Thr15Pro
NM_000307.5:c.43A>C MANE Select NP_000298.3:p.Thr15Pro
Search 100 bp 5'
Search 100 bp 3'