Canonical Allele Identifier: CA413751512
Gene: POU3F4 HGNC NCBI

Linked Data

gnomAD v4: X-83508751-G-C
MyVariant Identifiers: chrX:g.82763759G>C (hg19) chrX:g.83508751G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508751G>C , CM000685.2:g.83508751G>C GRCh38
NC_000023.10:g.82763759G>C , CM000685.1:g.82763759G>C GRCh37
NC_000023.9:g.82650415G>C NCBI36
NG_009936.2:g.5491G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.427G>C MANE Select ENSP00000495996.1:p.Gly143Arg
ENST00000373200.4:c.427G>C ENSP00000362296.2:p.Gly143Arg
NM_000307.4:c.427G>C NP_000298.3:p.Gly143Arg
NM_000307.5:c.427G>C MANE Select NP_000298.3:p.Gly143Arg
Search 100 bp 5'
Search 100 bp 3'