Canonical Allele Identifier: CA2584327950
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521845G>C , CM000681.2:g.33521845G>C GRCh38
NC_000019.9:g.34012751G>C , CM000681.1:g.34012751G>C GRCh37
NC_000019.8:g.38704591G>C NCBI36
NG_013358.1:g.5049C>G
NG_013358.2:g.5049C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-85C>G NP_000276.2:n.-85C>G
NM_001166056.1:c.-85C>G NP_001159528.1:n.-85C>G
NM_001166057.1:c.-85C>G NP_001159529.1:n.-85C>G