Canonical Allele Identifier: CA413751205
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1163443982
MyVariant Identifiers: chrX:g.82763617T>G (hg19) chrX:g.83508609T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508609T>G , CM000685.2:g.83508609T>G GRCh38
NC_000023.10:g.82763617T>G , CM000685.1:g.82763617T>G GRCh37
NC_000023.9:g.82650273T>G NCBI36
NG_009936.2:g.5349T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.285T>G MANE Select ENSP00000495996.1:p.His95Gln
ENST00000373200.4:c.285T>G ENSP00000362296.2:p.His95Gln
NM_000307.4:c.285T>G NP_000298.3:p.His95Gln
NM_000307.5:c.285T>G MANE Select NP_000298.3:p.His95Gln
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Search 100 bp 3'