Canonical Allele Identifier: CA413752472
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1260538264
gnomAD v2: X-82764188-G-C
gnomAD v4: X-83509180-G-C
MyVariant Identifiers: chrX:g.82764188G>C (hg19) chrX:g.83509180G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83509180G>C , CM000685.2:g.83509180G>C GRCh38
NC_000023.10:g.82764188G>C , CM000685.1:g.82764188G>C GRCh37
NC_000023.9:g.82650844G>C NCBI36
NG_009936.2:g.5920G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.856G>C MANE Select ENSP00000495996.1:p.Glu286Gln
ENST00000373200.4:c.856G>C ENSP00000362296.2:p.Glu286Gln
NM_000307.4:c.856G>C NP_000298.3:p.Glu286Gln
NM_000307.5:c.856G>C MANE Select NP_000298.3:p.Glu286Gln
Search 100 bp 5'
Search 100 bp 3'