Canonical Allele Identifier: CA447097651
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719392T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339829T>G , CM000667.2:g.146339829T>G GRCh38
NC_000005.9:g.145719392T>G , CM000667.1:g.145719392T>G GRCh37
NC_000005.8:g.145699585T>G NCBI36
NG_011885.1:g.5806T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.402T>G MANE Select ENSP00000495718.1:p.Ala134=
ENST00000230732.4:c.402T>G ENSP00000230732.4:p.Ala134=
NM_002700.2:c.402T>G NP_002691.1:p.Ala134=
NM_002700.3:c.402T>G MANE Select NP_002691.1:p.Ala134=
Search 100 bp 5'
Search 100 bp 3'