Canonical Allele Identifier: CA413750739
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1160172993
gnomAD v2: X-82763406-T-G
gnomAD v4: X-83508398-T-G
MyVariant Identifiers: chrX:g.82763406T>G (hg19) chrX:g.83508398T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508398T>G , CM000685.2:g.83508398T>G GRCh38
NC_000023.10:g.82763406T>G , CM000685.1:g.82763406T>G GRCh37
NC_000023.9:g.82650062T>G NCBI36
NG_009936.2:g.5138T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.74T>G MANE Select ENSP00000495996.1:p.Met25Arg
ENST00000373200.4:c.74T>G ENSP00000362296.2:p.Met25Arg
NM_000307.4:c.74T>G NP_000298.3:p.Met25Arg
NM_000307.5:c.74T>G MANE Select NP_000298.3:p.Met25Arg
Search 100 bp 5'
Search 100 bp 3'