Canonical Allele Identifier: CA820105847
Gene: PEX3 HGNC NCBI

Linked Data

dbSNP Id: rs1222146604
MyVariant Identifiers: chr6:g.143810668C>T (hg19) chr6:g.143489531C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143489531C>T , CM000668.2:g.143489531C>T GRCh38
NC_000006.11:g.143810668C>T , CM000668.1:g.143810668C>T GRCh37
NC_000006.10:g.143852361C>T NCBI36
NG_008459.1:g.43751C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.*305C>T MANE Select ENSP00000356563.4:n.*305C>T
ENST00000367591.4:c.*305C>T ENSP00000356563.4:n.*305C>T
NM_003630.2:c.*305C>T NP_003621.1:n.*305C>T
NM_003630.3:c.*305C>T MANE Select NP_003621.1:n.*305C>T
Search 100 bp 5'
Search 100 bp 3'