Canonical Allele Identifier: CA332228287
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1019020002
MyVariant Identifiers: chrX:g.82763303A>T (hg19) chrX:g.83508295A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508295A>T , CM000685.2:g.83508295A>T GRCh38
NC_000023.10:g.82763303A>T , CM000685.1:g.82763303A>T GRCh37
NC_000023.9:g.82649959A>T NCBI36
NG_009936.2:g.5035A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.-30A>T MANE Select ENSP00000495996.1:n.-30A>T
ENST00000373200.4:c.-30A>T ENSP00000362296.2:n.-30A>T
NM_000307.4:c.-30A>T NP_000298.3:n.-30A>T
NM_000307.5:c.-30A>T MANE Select NP_000298.3:n.-30A>T
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