Canonical Allele Identifier: CA447097723
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719497T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339934T>A , CM000667.2:g.146339934T>A GRCh38
NC_000005.9:g.145719497T>A , CM000667.1:g.145719497T>A GRCh37
NC_000005.8:g.145699690T>A NCBI36
NG_011885.1:g.5911T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.507T>A MANE Select ENSP00000495718.1:p.Pro169=
ENST00000230732.4:c.507T>A ENSP00000230732.4:p.Pro169=
NM_002700.2:c.507T>A NP_002691.1:p.Pro169=
NM_002700.3:c.507T>A MANE Select NP_002691.1:p.Pro169=