Canonical Allele Identifier: CA517478682
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs374967521
gnomAD v2: X-82763301-A-G
gnomAD v4: X-83508293-A-G
MyVariant Identifiers: chrX:g.82763301A>G (hg19) chrX:g.83508293A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508293A>G , CM000685.2:g.83508293A>G GRCh38
NC_000023.10:g.82763301A>G , CM000685.1:g.82763301A>G GRCh37
NC_000023.9:g.82649957A>G NCBI36
NG_009936.2:g.5033A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.-32A>G MANE Select ENSP00000495996.1:n.-32A>G
ENST00000373200.4:c.-32A>G ENSP00000362296.2:n.-32A>G
NM_000307.4:c.-32A>G NP_000298.3:n.-32A>G
NM_000307.5:c.-32A>G MANE Select NP_000298.3:n.-32A>G
Search 100 bp 5'
Search 100 bp 3'