Canonical Allele Identifier: CA517479160
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs2147996742
MyVariant Identifiers: chrX:g.82764086C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83509078C>T , CM000685.2:g.83509078C>T GRCh38
NC_000023.10:g.82764086C>T , CM000685.1:g.82764086C>T GRCh37
NC_000023.9:g.82650742C>T NCBI36
NG_009936.2:g.5818C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.754C>T MANE Select ENSP00000495996.1:p.Leu252=
ENST00000373200.4:c.754C>T ENSP00000362296.2:p.Leu252=
NM_000307.4:c.754C>T NP_000298.3:p.Leu252=
NM_000307.5:c.754C>T MANE Select NP_000298.3:p.Leu252=