Canonical Allele Identifier: CA2584328011
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521890A>C , CM000681.2:g.33521890A>C GRCh38
NC_000019.9:g.34012796A>C , CM000681.1:g.34012796A>C GRCh37
NC_000019.8:g.38704636A>C NCBI36
NG_013358.1:g.5004T>G
NG_013358.2:g.5004T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-130T>G NP_000276.2:n.-130T>G
NM_001166056.1:c.-130T>G NP_001159528.1:n.-130T>G
NM_001166057.1:c.-130T>G NP_001159529.1:n.-130T>G