Canonical Allele Identifier: CA2576747113
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521837A>G , CM000681.2:g.33521837A>G GRCh38
NC_000019.9:g.34012743A>G , CM000681.1:g.34012743A>G GRCh37
NC_000019.8:g.38704583A>G NCBI36
NG_013358.1:g.5057T>C
NG_013358.2:g.5057T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-77T>C NP_000276.2:n.-77T>C
NM_001166056.1:c.-77T>C NP_001159528.1:n.-77T>C
NM_001166057.1:c.-77T>C NP_001159529.1:n.-77T>C