Canonical Allele Identifier: CA361620298
Gene: POU4F3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339666A>G , CM000667.2:g.146339666A>G GRCh38
NC_000005.9:g.145719229A>G , CM000667.1:g.145719229A>G GRCh37
NC_000005.8:g.145699422A>G NCBI36
NG_011885.1:g.5643A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.239A>G MANE Select ENSP00000495718.1:p.Tyr80Cys
ENST00000230732.4:c.239A>G ENSP00000230732.4:p.Tyr80Cys
NM_002700.2:c.239A>G NP_002691.1:p.Tyr80Cys
NM_002700.3:c.239A>G MANE Select NP_002691.1:p.Tyr80Cys