Canonical Allele Identifier: CA881625051
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs886054338
gnomAD v3: 19-33521890-A-T
gnomAD v4: 19-33521890-A-T
MyVariant Identifiers: chr19:g.34012796A>T (hg19) chr19:g.33521890A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521890A>T , CM000681.2:g.33521890A>T GRCh38
NC_000019.9:g.34012796A>T , CM000681.1:g.34012796A>T GRCh37
NC_000019.8:g.38704636A>T NCBI36
NG_013358.1:g.5004T>A
NG_013358.2:g.5004T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-130T>A NP_000276.2:n.-130T>A
NM_001166056.1:c.-130T>A NP_001159528.1:n.-130T>A
NM_001166057.1:c.-130T>A NP_001159529.1:n.-130T>A
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