Canonical Allele Identifier: CA447097612

Gene: POU4F3

Linked Data

• dbSNP Id: rs1272379464
• MyVariant Identifiers: chr5:g.145719344C>T (hg19) ; chr5:g.146339781C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146339781C>T , CM000667.2:g.146339781C>T	GRCh38
NC_000005.9:g.145719344C>T , CM000667.1:g.145719344C>T	GRCh37
NC_000005.8:g.145699537C>T	NCBI36
NG_011885.1:g.5758C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646991.2:c.354C>T MANE Select	ENSP00000495718.1:p.Asp118=
ENST00000230732.4:c.354C>T	ENSP00000230732.4:p.Asp118=
NM_002700.2:c.354C>T	NP_002691.1:p.Asp118=
NM_002700.3:c.354C>T MANE Select	NP_002691.1:p.Asp118=