Canonical Allele Identifier: CA2576747133
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521855G>T , CM000681.2:g.33521855G>T GRCh38
NC_000019.9:g.34012761G>T , CM000681.1:g.34012761G>T GRCh37
NC_000019.8:g.38704601G>T NCBI36
NG_013358.1:g.5039C>A
NG_013358.2:g.5039C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-95C>A NP_000276.2:n.-95C>A
NM_001166056.1:c.-95C>A NP_001159528.1:n.-95C>A
NM_001166057.1:c.-95C>A NP_001159529.1:n.-95C>A