Canonical Allele Identifier: CA447097719
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719494C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339931C>A , CM000667.2:g.146339931C>A GRCh38
NC_000005.9:g.145719494C>A , CM000667.1:g.145719494C>A GRCh37
NC_000005.8:g.145699687C>A NCBI36
NG_011885.1:g.5908C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.504C>A MANE Select ENSP00000495718.1:p.Ala168=
ENST00000230732.4:c.504C>A ENSP00000230732.4:p.Ala168=
NM_002700.2:c.504C>A NP_002691.1:p.Ala168=
NM_002700.3:c.504C>A MANE Select NP_002691.1:p.Ala168=
Search 100 bp 5'
Search 100 bp 3'