Canonical Allele Identifier: CA3491129
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs140857174

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339850C>T , CM000667.2:g.146339850C>T GRCh38
NC_000005.9:g.145719413C>T , CM000667.1:g.145719413C>T GRCh37
NC_000005.8:g.145699606C>T NCBI36
NG_011885.1:g.5827C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.423C>T MANE Select ENSP00000495718.1:p.Pro141=
ENST00000230732.4:c.423C>T ENSP00000230732.4:p.Pro141=
NM_002700.2:c.423C>T NP_002691.1:p.Pro141=
NM_002700.3:c.423C>T MANE Select NP_002691.1:p.Pro141=