Canonical Allele Identifier: CA115372
Gene: PEX26 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 2156
ClinVar RCV Id: RCV000002239
dbSNP Id: rs74315506

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078378T>C , CM000684.2:g.18078378T>C GRCh38
NC_000022.10:g.18561144T>C , CM000684.1:g.18561144T>C GRCh37
NC_000022.9:g.16941144T>C NCBI36
NG_008339.1:g.5459T>C

Transcript Alleles

HGVS Amino-acid change
NM_001127649.2:c.2T>C VV
NM_001199319.1:c.2T>C VV
NM_017929.5:c.2T>C VV
ENST00000329627.11:c.2T>C
ENST00000399744.7:c.2T>C
ENST00000428061.2:n.2T>C
ENST00000474897.5:c.2T>C
ENST00000610387.4:c.2T>C