Canonical Allele Identifier: CA361620522
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1306842803

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339776G>T , CM000667.2:g.146339776G>T GRCh38
NC_000005.9:g.145719339G>T , CM000667.1:g.145719339G>T GRCh37
NC_000005.8:g.145699532G>T NCBI36
NG_011885.1:g.5753G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.349G>T MANE Select ENSP00000495718.1:p.Gly117Cys
ENST00000230732.4:c.349G>T ENSP00000230732.4:p.Gly117Cys
NM_002700.2:c.349G>T NP_002691.1:p.Gly117Cys
NM_002700.3:c.349G>T MANE Select NP_002691.1:p.Gly117Cys