Canonical Allele Identifier: CA413751938
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763952A>T (hg19) chrX:g.83508944A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508944A>T , CM000685.2:g.83508944A>T GRCh38
NC_000023.10:g.82763952A>T , CM000685.1:g.82763952A>T GRCh37
NC_000023.9:g.82650608A>T NCBI36
NG_009936.2:g.5684A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.620A>T MANE Select ENSP00000495996.1:p.Lys207Met
ENST00000373200.4:c.620A>T ENSP00000362296.2:p.Lys207Met
NM_000307.4:c.620A>T NP_000298.3:p.Lys207Met
NM_000307.5:c.620A>T MANE Select NP_000298.3:p.Lys207Met
Search 100 bp 5'
Search 100 bp 3'