Canonical Allele Identifier: CA361621751
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1581278691
gnomAD v4: 5-146340089-G-A
MyVariant Identifiers: chr5:g.145719652G>A (hg19) chr5:g.146340089G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340089G>A , CM000667.2:g.146340089G>A GRCh38
NC_000005.9:g.145719652G>A , CM000667.1:g.145719652G>A GRCh37
NC_000005.8:g.145699845G>A NCBI36
NG_011885.1:g.6066G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.662G>A MANE Select ENSP00000495718.1:p.Gly221Asp
ENST00000230732.4:c.662G>A ENSP00000230732.4:p.Gly221Asp
NM_002700.2:c.662G>A NP_002691.1:p.Gly221Asp
NM_002700.3:c.662G>A MANE Select NP_002691.1:p.Gly221Asp
Search 100 bp 5'
Search 100 bp 3'