Canonical Allele Identifier: CA2814189181

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521859A>G , CM000681.2:g.33521859A>G	GRCh38
NC_000019.9:g.34012765A>G , CM000681.1:g.34012765A>G	GRCh37
NC_000019.8:g.38704605A>G	NCBI36
NG_013358.1:g.5035T>C
NG_013358.2:g.5035T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000285.3:c.-99T>C	NP_000276.2:n.-99T>C
NM_001166056.1:c.-99T>C	NP_001159528.1:n.-99T>C
NM_001166057.1:c.-99T>C	NP_001159529.1:n.-99T>C