Canonical Allele Identifier: CA2584327959
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521853C>A , CM000681.2:g.33521853C>A GRCh38
NC_000019.9:g.34012759C>A , CM000681.1:g.34012759C>A GRCh37
NC_000019.8:g.38704599C>A NCBI36
NG_013358.1:g.5041G>T
NG_013358.2:g.5041G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-93G>T NP_000276.2:n.-93G>T
NM_001166056.1:c.-93G>T NP_001159528.1:n.-93G>T
NM_001166057.1:c.-93G>T NP_001159529.1:n.-93G>T