Canonical Allele Identifier: CA292020758
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs557849868
gnomAD v3: 17-58281664-A-C
gnomAD v4: 17-58281664-A-C
MyVariant Identifiers: chr17:g.56359025A>C (hg19) chr17:g.58281664A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281664A>C , CM000679.2:g.58281664A>C GRCh38
NC_000017.10:g.56359025A>C , CM000679.1:g.56359025A>C GRCh37
NC_000017.9:g.53714024A>C NCBI36
NG_009629.1:g.4272T>G , LRG_84:g.4272T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-595T>G XP_011523123.1:n.71-595T>G
XM_011524823.1:c.71-595T>G XP_011523125.1:n.71-595T>G
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