Canonical Allele Identifier: CA365887509
Gene: PEX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098397
ClinVar RCV Id: RCV003019177

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485210C>T , CM000668.2:g.143485210C>T GRCh38
NC_000006.11:g.143806347C>T , CM000668.1:g.143806347C>T GRCh37
NC_000006.10:g.143848040C>T NCBI36
NG_008459.1:g.39430C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.1000C>T MANE Select ENSP00000356563.4:p.His334Tyr
ENST00000367591.4:c.1000C>T ENSP00000356563.4:p.His334Tyr
ENST00000585848.1:n.139C>T
NM_003630.2:c.1000C>T NP_003621.1:p.His334Tyr
NM_003630.3:c.1000C>T MANE Select NP_003621.1:p.His334Tyr