Canonical Allele Identifier: CA292020529
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs985924901
gnomAD v3: 17-58281260-A-G
gnomAD v4: 17-58281260-A-G
MyVariant Identifiers: chr17:g.56358621A>G (hg19) chr17:g.58281260A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281260A>G , CM000679.2:g.58281260A>G GRCh38
NC_000017.10:g.56358621A>G , CM000679.1:g.56358621A>G GRCh37
NC_000017.9:g.53713620A>G NCBI36
NG_009629.1:g.4676T>C , LRG_84:g.4676T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-191T>C XP_011523123.1:n.71-191T>C
XM_011524823.1:c.71-191T>C XP_011523125.1:n.71-191T>C
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