Canonical Allele Identifier: CA452462462
Gene: PEX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.143806253T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485116T>G , CM000668.2:g.143485116T>G GRCh38
NC_000006.11:g.143806253T>G , CM000668.1:g.143806253T>G GRCh37
NC_000006.10:g.143847946T>G NCBI36
NG_008459.1:g.39336T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.942-36T>G MANE Select ENSP00000356563.4:n.942-36T>G
ENST00000367591.4:c.942-36T>G ENSP00000356563.4:n.942-36T>G
ENST00000585848.1:n.45T>G
NM_003630.2:c.942-36T>G NP_003621.1:n.942-36T>G
NM_003630.3:c.942-36T>G MANE Select NP_003621.1:n.942-36T>G
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