Canonical Allele Identifier: CA361620605

Gene: POU4F3

Linked Data

• dbSNP Id: rs1458021936
• MyVariant Identifiers: chr5:g.145719381G>A (hg19) ; chr5:g.146339818G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146339818G>A , CM000667.2:g.146339818G>A	GRCh38
NC_000005.9:g.145719381G>A , CM000667.1:g.145719381G>A	GRCh37
NC_000005.8:g.145699574G>A	NCBI36
NG_011885.1:g.5795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646991.2:c.391G>A MANE Select	ENSP00000495718.1:p.Gly131Ser
ENST00000230732.4:c.391G>A	ENSP00000230732.4:p.Gly131Ser
NM_002700.2:c.391G>A	NP_002691.1:p.Gly131Ser
NM_002700.3:c.391G>A MANE Select	NP_002691.1:p.Gly131Ser