Canonical Allele Identifier: CA361620786
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1167694009
gnomAD v3: 5-146339905-G-A
gnomAD v4: 5-146339905-G-A
MyVariant Identifiers: chr5:g.145719468G>A (hg19) chr5:g.146339905G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339905G>A , CM000667.2:g.146339905G>A GRCh38
NC_000005.9:g.145719468G>A , CM000667.1:g.145719468G>A GRCh37
NC_000005.8:g.145699661G>A NCBI36
NG_011885.1:g.5882G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.478G>A MANE Select ENSP00000495718.1:p.Gly160Ser
ENST00000230732.4:c.478G>A ENSP00000230732.4:p.Gly160Ser
NM_002700.2:c.478G>A NP_002691.1:p.Gly160Ser
NM_002700.3:c.478G>A MANE Select NP_002691.1:p.Gly160Ser
Search 100 bp 5'
Search 100 bp 3'