Canonical Allele Identifier: CA447097727
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719500T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339937T>C , CM000667.2:g.146339937T>C GRCh38
NC_000005.9:g.145719500T>C , CM000667.1:g.145719500T>C GRCh37
NC_000005.8:g.145699693T>C NCBI36
NG_011885.1:g.5914T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.510T>C MANE Select ENSP00000495718.1:p.His170=
ENST00000230732.4:c.510T>C ENSP00000230732.4:p.His170=
NM_002700.2:c.510T>C NP_002691.1:p.His170=
NM_002700.3:c.510T>C MANE Select NP_002691.1:p.His170=