Canonical Allele Identifier: CA583367321

Gene: PEX2

Linked Data

• dbSNP Id: rs1380044514
• gnomAD v2: 8-77895466-T-C
• gnomAD v4: 8-76983230-T-C
• MyVariant Identifiers: chr8:g.77895466T>C (hg19) ; chr8:g.76983230T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983230T>C , CM000670.2:g.76983230T>C	GRCh38
NC_000008.10:g.77895466T>C , CM000670.1:g.77895466T>C	GRCh37
NC_000008.9:g.78058021T>C	NCBI36
NG_008371.1:g.22059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357039.9:c.*31A>G MANE Select	ENSP00000349543.4:n.*31A>G
ENST00000357039.8:c.*31A>G	ENSP00000349543.4:n.*31A>G
ENST00000520103.5:c.*31A>G	ENSP00000428590.1:n.*31A>G
ENST00000522527.5:c.*31A>G	ENSP00000428638.1:n.*31A>G
NM_000318.2:c.*31A>G	NP_000309.1:n.*31A>G
NM_001079867.1:c.*31A>G	NP_001073336.1:n.*31A>G
NM_001172086.1:c.*31A>G	NP_001165557.1:n.*31A>G
NM_001172087.1:c.*31A>G	NP_001165558.1:n.*31A>G
NM_000318.3:c.*31A>G MANE Select	NP_000309.2:n.*31A>G
NM_001079867.2:c.*31A>G	NP_001073336.2:n.*31A>G
NM_001172086.2:c.*31A>G	NP_001165557.2:n.*31A>G
NM_001172087.2:c.*31A>G	NP_001165558.2:n.*31A>G