Canonical Allele Identifier: CA452462466
Gene: PEX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.143806255T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485118T>A , CM000668.2:g.143485118T>A GRCh38
NC_000006.11:g.143806255T>A , CM000668.1:g.143806255T>A GRCh37
NC_000006.10:g.143847948T>A NCBI36
NG_008459.1:g.39338T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.942-34T>A MANE Select ENSP00000356563.4:n.942-34T>A
ENST00000367591.4:c.942-34T>A ENSP00000356563.4:n.942-34T>A
ENST00000585848.1:n.47T>A
NM_003630.2:c.942-34T>A NP_003621.1:n.942-34T>A
NM_003630.3:c.942-34T>A MANE Select NP_003621.1:n.942-34T>A