Canonical Allele Identifier: CA517478489
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1248407740
MyVariant Identifiers: chrX:g.82763260C>A (hg19) chrX:g.83508252C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508252C>A , CM000685.2:g.83508252C>A GRCh38
NC_000023.10:g.82763260C>A , CM000685.1:g.82763260C>A GRCh37
NC_000023.9:g.82649916C>A NCBI36
NG_009936.2:g.4992C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373200.4:c.-73C>A ENSP00000362296.2:n.-73C>A
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