Canonical Allele Identifier: CA452462456
Gene: PEX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.143806251C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485114C>G , CM000668.2:g.143485114C>G GRCh38
NC_000006.11:g.143806251C>G , CM000668.1:g.143806251C>G GRCh37
NC_000006.10:g.143847944C>G NCBI36
NG_008459.1:g.39334C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.942-38C>G MANE Select ENSP00000356563.4:n.942-38C>G
ENST00000367591.4:c.942-38C>G ENSP00000356563.4:n.942-38C>G
ENST00000585848.1:n.43C>G
NM_003630.2:c.942-38C>G NP_003621.1:n.942-38C>G
NM_003630.3:c.942-38C>G MANE Select NP_003621.1:n.942-38C>G