Canonical Allele Identifier: CA517478748
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1925821976
gnomAD v4: X-83508303-T-C
MyVariant Identifiers: chrX:g.82763311T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508303T>C , CM000685.2:g.83508303T>C GRCh38
NC_000023.10:g.82763311T>C , CM000685.1:g.82763311T>C GRCh37
NC_000023.9:g.82649967T>C NCBI36
NG_009936.2:g.5043T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.-22T>C MANE Select ENSP00000495996.1:n.-22T>C
ENST00000373200.4:c.-22T>C ENSP00000362296.2:n.-22T>C
NM_000307.4:c.-22T>C NP_000298.3:n.-22T>C
NM_000307.5:c.-22T>C MANE Select NP_000298.3:n.-22T>C
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