Canonical Allele Identifier: CA292020568
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs934954738

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281335A>G , CM000679.2:g.58281335A>G GRCh38
NC_000017.10:g.56358696A>G , CM000679.1:g.56358696A>G GRCh37
NC_000017.9:g.53713695A>G NCBI36
NG_009629.1:g.4601T>C , LRG_84:g.4601T>C

Transcript Alleles

HGVS Amino-acid change
XM_011524821.1:c.71-266T>C XP_011523123.1:n.71-266T>C
XM_011524823.1:c.71-266T>C XP_011523125.1:n.71-266T>C