Canonical Allele Identifier: CA447097892
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1760431134
MyVariant Identifiers: chr5:g.145719656G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340093G>A , CM000667.2:g.146340093G>A GRCh38
NC_000005.9:g.145719656G>A , CM000667.1:g.145719656G>A GRCh37
NC_000005.8:g.145699849G>A NCBI36
NG_011885.1:g.6070G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.666G>A MANE Select ENSP00000495718.1:p.Ser222=
ENST00000230732.4:c.666G>A ENSP00000230732.4:p.Ser222=
NM_002700.2:c.666G>A NP_002691.1:p.Ser222=
NM_002700.3:c.666G>A MANE Select NP_002691.1:p.Ser222=