Canonical Allele Identifier: CA413750635
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763357T>G (hg19) chrX:g.83508349T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508349T>G , CM000685.2:g.83508349T>G GRCh38
NC_000023.10:g.82763357T>G , CM000685.1:g.82763357T>G GRCh37
NC_000023.9:g.82650013T>G NCBI36
NG_009936.2:g.5089T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.25T>G MANE Select ENSP00000495996.1:p.Tyr9Asp
ENST00000373200.4:c.25T>G ENSP00000362296.2:p.Tyr9Asp
NM_000307.4:c.25T>G NP_000298.3:p.Tyr9Asp
NM_000307.5:c.25T>G MANE Select NP_000298.3:p.Tyr9Asp
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Search 100 bp 3'