Canonical Allele Identifier: CA446918680
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719227C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339664C>A , CM000667.2:g.146339664C>A GRCh38
NC_000005.9:g.145719227C>A , CM000667.1:g.145719227C>A GRCh37
NC_000005.8:g.145699420C>A NCBI36
NG_011885.1:g.5641C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.237C>A MANE Select ENSP00000495718.1:p.Thr79=
ENST00000230732.4:c.237C>A ENSP00000230732.4:p.Thr79=
NM_002700.2:c.237C>A NP_002691.1:p.Thr79=
NM_002700.3:c.237C>A MANE Select NP_002691.1:p.Thr79=
Search 100 bp 5'
Search 100 bp 3'