Canonical Allele Identifier: CA447097692
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719461G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339898G>A , CM000667.2:g.146339898G>A GRCh38
NC_000005.9:g.145719461G>A , CM000667.1:g.145719461G>A GRCh37
NC_000005.8:g.145699654G>A NCBI36
NG_011885.1:g.5875G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.471G>A MANE Select ENSP00000495718.1:p.Gln157=
ENST00000230732.4:c.471G>A ENSP00000230732.4:p.Gln157=
NM_002700.2:c.471G>A NP_002691.1:p.Gln157=
NM_002700.3:c.471G>A MANE Select NP_002691.1:p.Gln157=
Search 100 bp 5'
Search 100 bp 3'