Canonical Allele Identifier: CA881625034
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1241328091
gnomAD v3: 19-33521871-AC-A
gnomAD v4: 19-33521871-AC-A
MyVariant Identifiers: chr19:g.34012778del (hg19) chr19:g.33521872del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521874del , CM000681.2:g.33521874del GRCh38
NC_000019.9:g.34012780del , CM000681.1:g.34012780del GRCh37
NC_000019.8:g.38704620del NCBI36
NG_013358.1:g.5022del
NG_013358.2:g.5022del

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-112del NP_000276.2:n.-112del
NM_001166056.1:c.-112del NP_001159528.1:n.-112del
NM_001166057.1:c.-112del NP_001159529.1:n.-112del
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