Canonical Allele Identifier: CA413751551
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs746754567
gnomAD v2: X-82763778-G-C
gnomAD v3: X-83508770-G-C
gnomAD v4: X-83508770-G-C
MyVariant Identifiers: chrX:g.82763778G>C (hg19) chrX:g.83508770G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508770G>C , CM000685.2:g.83508770G>C GRCh38
NC_000023.10:g.82763778G>C , CM000685.1:g.82763778G>C GRCh37
NC_000023.9:g.82650434G>C NCBI36
NG_009936.2:g.5510G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.446G>C MANE Select ENSP00000495996.1:p.Gly149Ala
ENST00000373200.4:c.446G>C ENSP00000362296.2:p.Gly149Ala
NM_000307.4:c.446G>C NP_000298.3:p.Gly149Ala
NM_000307.5:c.446G>C MANE Select NP_000298.3:p.Gly149Ala
Search 100 bp 5'
Search 100 bp 3'