Canonical Allele Identifier: CA292020572

Gene: MPO

Linked Data

• dbSNP Id: rs935818861
• MyVariant Identifiers: chr17:g.56358702T>G (hg19) ; chr17:g.58281341T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58281341T>G , CM000679.2:g.58281341T>G	GRCh38
NC_000017.10:g.56358702T>G , CM000679.1:g.56358702T>G	GRCh37
NC_000017.9:g.53713701T>G	NCBI36
NG_009629.1:g.4595A>C , LRG_84:g.4595A>C

Transcript Alleles

HGVS	Amino-acid change
XM_011524821.1:c.71-272A>C	XP_011523123.1:n.71-272A>C
XM_011524823.1:c.71-272A>C	XP_011523125.1:n.71-272A>C