Canonical Allele Identifier: CA2584327988
Gene: PEPD HGNC NCBI

Linked Data

gnomAD v4: 19-33521872-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521872C>G , CM000681.2:g.33521872C>G GRCh38
NC_000019.9:g.34012778C>G , CM000681.1:g.34012778C>G GRCh37
NC_000019.8:g.38704618C>G NCBI36
NG_013358.1:g.5022G>C
NG_013358.2:g.5022G>C

Transcript Alleles

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