Canonical Allele Identifier: CA292020660
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs531557147

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281472T>C , CM000679.2:g.58281472T>C GRCh38
NC_000017.10:g.56358833T>C , CM000679.1:g.56358833T>C GRCh37
NC_000017.9:g.53713832T>C NCBI36
NG_009629.1:g.4464A>G , LRG_84:g.4464A>G

Transcript Alleles

HGVS Amino-acid change
XM_011524821.1:c.71-403A>G XP_011523123.1:n.71-403A>G
XM_011524823.1:c.71-403A>G XP_011523125.1:n.71-403A>G