Canonical Allele Identifier: CA2576747125
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521848G>A , CM000681.2:g.33521848G>A GRCh38
NC_000019.9:g.34012754G>A , CM000681.1:g.34012754G>A GRCh37
NC_000019.8:g.38704594G>A NCBI36
NG_013358.1:g.5046C>T
NG_013358.2:g.5046C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-88C>T NP_000276.2:n.-88C>T
NM_001166056.1:c.-88C>T NP_001159528.1:n.-88C>T
NM_001166057.1:c.-88C>T NP_001159529.1:n.-88C>T