Canonical Allele Identifier: CA292020594

Gene: MPO

Linked Data

• dbSNP Id: rs891695460
• gnomAD v3: 17-58281346-G-T
• gnomAD v4: 17-58281346-G-T
• MyVariant Identifiers: chr17:g.56358707G>T (hg19) ; chr17:g.58281346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58281346G>T , CM000679.2:g.58281346G>T	GRCh38
NC_000017.10:g.56358707G>T , CM000679.1:g.56358707G>T	GRCh37
NC_000017.9:g.53713706G>T	NCBI36
NG_009629.1:g.4590C>A , LRG_84:g.4590C>A

Transcript Alleles

HGVS	Amino-acid change
XM_011524821.1:c.71-277C>A	XP_011523123.1:n.71-277C>A
XM_011524823.1:c.71-277C>A	XP_011523125.1:n.71-277C>A