Canonical Allele Identifier: CA307575769

Gene: PEPD

Linked Data

• dbSNP Id: rs1035200598
• gnomAD v4: 19-33521891-A-G
• MyVariant Identifiers: chr19:g.34012797A>G (hg19) ; chr19:g.33521891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521891A>G , CM000681.2:g.33521891A>G	GRCh38
NC_000019.9:g.34012797A>G , CM000681.1:g.34012797A>G	GRCh37
NC_000019.8:g.38704637A>G	NCBI36
NG_013358.1:g.5003T>C
NG_013358.2:g.5003T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000285.3:c.-131T>C	NP_000276.2:n.-131T>C
NM_001166056.1:c.-131T>C	NP_001159528.1:n.-131T>C
NM_001166057.1:c.-131T>C	NP_001159529.1:n.-131T>C