Canonical Allele Identifier: CA361622663
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1760434770

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340262A>T , CM000667.2:g.146340262A>T GRCh38
NC_000005.9:g.145719825A>T , CM000667.1:g.145719825A>T GRCh37
NC_000005.8:g.145700018A>T NCBI36
NG_011885.1:g.6239A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.835A>T MANE Select ENSP00000495718.1:p.Thr279Ser
ENST00000230732.4:c.835A>T ENSP00000230732.4:p.Thr279Ser
NM_002700.2:c.835A>T NP_002691.1:p.Thr279Ser
NM_002700.3:c.835A>T MANE Select NP_002691.1:p.Thr279Ser