Canonical Allele Identifier: CA773487965

Gene: MPO

Linked Data

• dbSNP Id: rs1215211211
• gnomAD v3: 17-58281446-G-T
• gnomAD v4: 17-58281446-G-T
• MyVariant Identifiers: chr17:g.56358807G>T (hg19) ; chr17:g.58281446G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58281446G>T , CM000679.2:g.58281446G>T	GRCh38
NC_000017.10:g.56358807G>T , CM000679.1:g.56358807G>T	GRCh37
NC_000017.9:g.53713806G>T	NCBI36
NG_009629.1:g.4490C>A , LRG_84:g.4490C>A

Transcript Alleles

HGVS	Amino-acid change
XM_011524821.1:c.71-377C>A	XP_011523123.1:n.71-377C>A
XM_011524823.1:c.71-377C>A	XP_011523125.1:n.71-377C>A