Canonical Allele Identifier: CA517478696
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763767G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508759G>T , CM000685.2:g.83508759G>T GRCh38
NC_000023.10:g.82763767G>T , CM000685.1:g.82763767G>T GRCh37
NC_000023.9:g.82650423G>T NCBI36
NG_009936.2:g.5499G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.435G>T MANE Select ENSP00000495996.1:p.Leu145=
ENST00000373200.4:c.435G>T ENSP00000362296.2:p.Leu145=
NM_000307.4:c.435G>T NP_000298.3:p.Leu145=
NM_000307.5:c.435G>T MANE Select NP_000298.3:p.Leu145=
Search 100 bp 5'
Search 100 bp 3'