Canonical Allele Identifier: CA517478936
Gene: POU3F4 HGNC NCBI

Linked Data

gnomAD v4: X-83508342-G-T
MyVariant Identifiers: chrX:g.82763350G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508342G>T , CM000685.2:g.83508342G>T GRCh38
NC_000023.10:g.82763350G>T , CM000685.1:g.82763350G>T GRCh37
NC_000023.9:g.82650006G>T NCBI36
NG_009936.2:g.5082G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.18G>T MANE Select ENSP00000495996.1:p.Ser6=
ENST00000373200.4:c.18G>T ENSP00000362296.2:p.Ser6=
NM_000307.4:c.18G>T NP_000298.3:p.Ser6=
NM_000307.5:c.18G>T MANE Select NP_000298.3:p.Ser6=