Canonical Allele Identifier: CA3491131
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs368466009

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339855A>G , CM000667.2:g.146339855A>G GRCh38
NC_000005.9:g.145719418A>G , CM000667.1:g.145719418A>G GRCh37
NC_000005.8:g.145699611A>G NCBI36
NG_011885.1:g.5832A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.428A>G MANE Select ENSP00000495718.1:p.Gln143Arg
ENST00000230732.4:c.428A>G ENSP00000230732.4:p.Gln143Arg
NM_002700.2:c.428A>G NP_002691.1:p.Gln143Arg
NM_002700.3:c.428A>G MANE Select NP_002691.1:p.Gln143Arg