Canonical Allele Identifier: CA2576747136
Gene: PEPD HGNC NCBI

Linked Data

gnomAD v4: 19-33521860-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521860T>C , CM000681.2:g.33521860T>C GRCh38
NC_000019.9:g.34012766T>C , CM000681.1:g.34012766T>C GRCh37
NC_000019.8:g.38704606T>C NCBI36
NG_013358.1:g.5034A>G
NG_013358.2:g.5034A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-100A>G NP_000276.2:n.-100A>G
NM_001166056.1:c.-100A>G NP_001159528.1:n.-100A>G
NM_001166057.1:c.-100A>G NP_001159529.1:n.-100A>G
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