Canonical Allele Identifier: CA413751379
Gene: POU3F4 HGNC NCBI

Linked Data

dbSNP Id: rs1925835012

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508688C>T , CM000685.2:g.83508688C>T GRCh38
NC_000023.10:g.82763696C>T , CM000685.1:g.82763696C>T GRCh37
NC_000023.9:g.82650352C>T NCBI36
NG_009936.2:g.5428C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644024.2:c.364C>T MANE Select ENSP00000495996.1:p.Pro122Ser
ENST00000373200.4:c.364C>T ENSP00000362296.2:p.Pro122Ser
NM_000307.4:c.364C>T NP_000298.3:p.Pro122Ser
NM_000307.5:c.364C>T MANE Select NP_000298.3:p.Pro122Ser