Canonical Allele Identifier: CA881625019
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1157982445
gnomAD v4: 19-33521833-G-T
MyVariant Identifiers: chr19:g.34012739G>T (hg19) chr19:g.33521833G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521833G>T , CM000681.2:g.33521833G>T GRCh38
NC_000019.9:g.34012739G>T , CM000681.1:g.34012739G>T GRCh37
NC_000019.8:g.38704579G>T NCBI36
NG_013358.1:g.5061C>A
NG_013358.2:g.5061C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-73C>A NP_000276.2:n.-73C>A
NM_001166056.1:c.-73C>A NP_001159528.1:n.-73C>A
NM_001166057.1:c.-73C>A NP_001159529.1:n.-73C>A
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