Canonical Allele Identifier: CA292020239

Gene: MPO

Linked Data

• dbSNP Id: rs971769525
• MyVariant Identifiers: chr17:g.56358391C>T (hg19) ; chr17:g.58281030C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58281030C>T , CM000679.2:g.58281030C>T	GRCh38
NC_000017.10:g.56358391C>T , CM000679.1:g.56358391C>T	GRCh37
NC_000017.9:g.53713390C>T	NCBI36
NG_009629.1:g.4906G>A , LRG_84:g.4906G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011524821.1:c.110G>A	XP_011523123.1:p.Gly37Glu
XM_011524823.1:c.110G>A	XP_011523125.1:p.Gly37Glu