Canonical Allele Identifier: CA10462729
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs779934284
ExAC: X:82763358 A / C
gnomAD v2: X-82763358-A-C
gnomAD v4: X-83508350-A-C
MyVariant Identifiers: chrX:g.82763358A>C (hg19) chrX:g.83508350A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508350A>C , CM000685.2:g.83508350A>C GRCh38
NC_000023.10:g.82763358A>C , CM000685.1:g.82763358A>C GRCh37
NC_000023.9:g.82650014A>C NCBI36
NG_009936.2:g.5090A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.26A>C MANE Select ENSP00000495996.1:p.Tyr9Ser
ENST00000373200.4:c.26A>C ENSP00000362296.2:p.Tyr9Ser
NM_000307.4:c.26A>C NP_000298.3:p.Tyr9Ser
NM_000307.5:c.26A>C MANE Select NP_000298.3:p.Tyr9Ser
Search 100 bp 5'
Search 100 bp 3'