Canonical Allele Identifier: CA452462477
Gene: PEX3 HGNC NCBI

Linked Data

gnomAD v4: 6-143485121-G-T
MyVariant Identifiers: chr6:g.143806258G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485121G>T , CM000668.2:g.143485121G>T GRCh38
NC_000006.11:g.143806258G>T , CM000668.1:g.143806258G>T GRCh37
NC_000006.10:g.143847951G>T NCBI36
NG_008459.1:g.39341G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.942-31G>T MANE Select ENSP00000356563.4:n.942-31G>T
ENST00000367591.4:c.942-31G>T ENSP00000356563.4:n.942-31G>T
ENST00000585848.1:n.50G>T
NM_003630.2:c.942-31G>T NP_003621.1:n.942-31G>T
NM_003630.3:c.942-31G>T MANE Select NP_003621.1:n.942-31G>T
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