Canonical Allele Identifier: CA292020577

Gene: MPO

Linked Data

• dbSNP Id: rs1054716173
• gnomAD v3: 17-58281344-A-C
• gnomAD v4: 17-58281344-A-C
• MyVariant Identifiers: chr17:g.56358705A>C (hg19) ; chr17:g.58281344A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58281344A>C , CM000679.2:g.58281344A>C	GRCh38
NC_000017.10:g.56358705A>C , CM000679.1:g.56358705A>C	GRCh37
NC_000017.9:g.53713704A>C	NCBI36
NG_009629.1:g.4592T>G , LRG_84:g.4592T>G

Transcript Alleles

HGVS	Amino-acid change
XM_011524821.1:c.71-275T>G	XP_011523123.1:n.71-275T>G
XM_011524823.1:c.71-275T>G	XP_011523125.1:n.71-275T>G