Canonical Allele Identifier: CA361622661

Gene: POU4F3

Linked Data

• dbSNP Id: rs1760434770
• MyVariant Identifiers: chr5:g.145719825A>G (hg19) ; chr5:g.146340262A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646991.2:c.835A>G MANE Select	ENSP00000495718.1:p.Thr279Ala
ENST00000230732.4:c.835A>G	ENSP00000230732.4:p.Thr279Ala
NM_002700.2:c.835A>G	NP_002691.1:p.Thr279Ala
NM_002700.3:c.835A>G MANE Select	NP_002691.1:p.Thr279Ala