Canonical Allele Identifier: CA361622099
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs2126961820

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340163C>A , CM000667.2:g.146340163C>A GRCh38
NC_000005.9:g.145719726C>A , CM000667.1:g.145719726C>A GRCh37
NC_000005.8:g.145699919C>A NCBI36
NG_011885.1:g.6140C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.736C>A MANE Select ENSP00000495718.1:p.Pro246Thr
ENST00000230732.4:c.736C>A ENSP00000230732.4:p.Pro246Thr
NM_002700.2:c.736C>A NP_002691.1:p.Pro246Thr
NM_002700.3:c.736C>A MANE Select NP_002691.1:p.Pro246Thr