Canonical Allele Identifier: CA292020686
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs921994847
gnomAD v3: 17-58281583-A-T
gnomAD v4: 17-58281583-A-T
MyVariant Identifiers: chr17:g.56358944A>T (hg19) chr17:g.58281583A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281583A>T , CM000679.2:g.58281583A>T GRCh38
NC_000017.10:g.56358944A>T , CM000679.1:g.56358944A>T GRCh37
NC_000017.9:g.53713943A>T NCBI36
NG_009629.1:g.4353T>A , LRG_84:g.4353T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-514T>A XP_011523123.1:n.71-514T>A
XM_011524823.1:c.71-514T>A XP_011523125.1:n.71-514T>A
Search 100 bp 5'
Search 100 bp 3'