Canonical Allele Identifier: CA626724690
Gene: MPO HGNC NCBI

Linked Data

gnomAD v2: 17-56358348-G-T
gnomAD v4: 17-58280987-G-T
MyVariant Identifiers: chr17:g.56358348G>T (hg19) chr17:g.58280987G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280987G>T , CM000679.2:g.58280987G>T GRCh38
NC_000017.10:g.56358348G>T , CM000679.1:g.56358348G>T GRCh37
NC_000017.9:g.53713347G>T NCBI36
NG_009629.1:g.4949C>A , LRG_84:g.4949C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.153C>A XP_011523123.1:p.His51Gln
XM_011524823.1:c.153C>A XP_011523125.1:p.His51Gln
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