Canonical Allele Identifier: CA365887722
Gene: PEX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.143806378T>A (hg19) chr6:g.143485241T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485241T>A , CM000668.2:g.143485241T>A GRCh38
NC_000006.11:g.143806378T>A , CM000668.1:g.143806378T>A GRCh37
NC_000006.10:g.143848071T>A NCBI36
NG_008459.1:g.39461T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.1031T>A MANE Select ENSP00000356563.4:p.Phe344Tyr
ENST00000367591.4:c.1031T>A ENSP00000356563.4:p.Phe344Tyr
ENST00000585848.1:n.170T>A
NM_003630.2:c.1031T>A NP_003621.1:p.Phe344Tyr
NM_003630.3:c.1031T>A MANE Select NP_003621.1:p.Phe344Tyr
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