Canonical Allele Identifier: CA3491158
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs753663609

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339954G>A , CM000667.2:g.146339954G>A GRCh38
NC_000005.9:g.145719517G>A , CM000667.1:g.145719517G>A GRCh37
NC_000005.8:g.145699710G>A NCBI36
NG_011885.1:g.5931G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.527G>A MANE Select ENSP00000495718.1:p.Cys176Tyr
ENST00000230732.4:c.527G>A ENSP00000230732.4:p.Cys176Tyr
NM_002700.2:c.527G>A NP_002691.1:p.Cys176Tyr
NM_002700.3:c.527G>A MANE Select NP_002691.1:p.Cys176Tyr