Canonical Allele Identifier: CA452462471
Gene: PEX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.143806256C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485119C>G , CM000668.2:g.143485119C>G GRCh38
NC_000006.11:g.143806256C>G , CM000668.1:g.143806256C>G GRCh37
NC_000006.10:g.143847949C>G NCBI36
NG_008459.1:g.39339C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.942-33C>G MANE Select ENSP00000356563.4:n.942-33C>G
ENST00000367591.4:c.942-33C>G ENSP00000356563.4:n.942-33C>G
ENST00000585848.1:n.48C>G
NM_003630.2:c.942-33C>G NP_003621.1:n.942-33C>G
NM_003630.3:c.942-33C>G MANE Select NP_003621.1:n.942-33C>G