Canonical Allele Identifier: CA177659
Gene: POU4F3 HGNC NCBI

Linked Data

ClinVar Variation Id: 164983
ClinVar RCV Id: RCV000151676 RCV000974514 RCV001153512
dbSNP Id: rs61737151
ExAC: 5:145719653 C / A
gnomAD v2: 5-145719653-C-A
gnomAD v3: 5-146340090-C-A
gnomAD v4: 5-146340090-C-A
MyVariant Identifiers: chr5:g.145719653C>A (hg19) chr5:g.146340090C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340090C>A , CM000667.2:g.146340090C>A GRCh38
NC_000005.9:g.145719653C>A , CM000667.1:g.145719653C>A GRCh37
NC_000005.8:g.145699846C>A NCBI36
NG_011885.1:g.6067C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.663C>A MANE Select ENSP00000495718.1:p.Gly221=
ENST00000230732.4:c.663C>A ENSP00000230732.4:p.Gly221=
NM_002700.2:c.663C>A NP_002691.1:p.Gly221=
NM_002700.3:c.663C>A MANE Select NP_002691.1:p.Gly221=
Search 100 bp 5'
Search 100 bp 3'