Canonical Allele Identifier: CA2332763202
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1600184852
gnomAD v4: 19-33521856-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521856G>A , CM000681.2:g.33521856G>A GRCh38
NC_000019.9:g.34012762G>A , CM000681.1:g.34012762G>A GRCh37
NC_000019.8:g.38704602G>A NCBI36
NG_013358.1:g.5038C>T
NG_013358.2:g.5038C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-96C>T NP_000276.2:n.-96C>T
NM_001166056.1:c.-96C>T NP_001159528.1:n.-96C>T
NM_001166057.1:c.-96C>T NP_001159529.1:n.-96C>T
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