Canonical Allele Identifier: CA292020390

Gene: MPO

Linked Data

• dbSNP Id: rs906940629
• gnomAD v2: 17-56358547-G-A
• gnomAD v3: 17-58281186-G-A
• gnomAD v4: 17-58281186-G-A
• MyVariant Identifiers: chr17:g.56358547G>A (hg19) ; chr17:g.58281186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58281186G>A , CM000679.2:g.58281186G>A	GRCh38
NC_000017.10:g.56358547G>A , CM000679.1:g.56358547G>A	GRCh37
NC_000017.9:g.53713546G>A	NCBI36
NG_009629.1:g.4750C>T , LRG_84:g.4750C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_011524821.1:c.71-117C>T	XP_011523123.1:n.71-117C>T
XM_011524823.1:c.71-117C>T	XP_011523125.1:n.71-117C>T