Canonical Allele Identifier: CA413750696
Gene: POU3F4 HGNC NCBI

Linked Data

COSMIC: COSM4890356 COSM4890357
MyVariant Identifiers: chrX:g.82763385T>C (hg19) chrX:g.83508377T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508377T>C , CM000685.2:g.83508377T>C GRCh38
NC_000023.10:g.82763385T>C , CM000685.1:g.82763385T>C GRCh37
NC_000023.9:g.82650041T>C NCBI36
NG_009936.2:g.5117T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.53T>C MANE Select ENSP00000495996.1:p.Val18Ala
ENST00000373200.4:c.53T>C ENSP00000362296.2:p.Val18Ala
NM_000307.4:c.53T>C NP_000298.3:p.Val18Ala
NM_000307.5:c.53T>C MANE Select NP_000298.3:p.Val18Ala
Search 100 bp 5'
Search 100 bp 3'