Canonical Allele Identifier: CA632705482
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1555772665
gnomAD v2: 19-34012732-G-C
gnomAD v3: 19-33521826-G-C
gnomAD v4: 19-33521826-G-C
MyVariant Identifiers: chr19:g.34012732G>C (hg19) chr19:g.33521826G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521826G>C , CM000681.2:g.33521826G>C GRCh38
NC_000019.9:g.34012732G>C , CM000681.1:g.34012732G>C GRCh37
NC_000019.8:g.38704572G>C NCBI36
NG_013358.1:g.5068C>G
NG_013358.2:g.5068C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-66C>G NP_000276.2:n.-66C>G
NM_001166056.1:c.-66C>G NP_001159528.1:n.-66C>G
NM_001166057.1:c.-66C>G NP_001159529.1:n.-66C>G
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