Canonical Allele Identifier: CA292020421
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1033846764
gnomAD v2: 17-56358559-C-T
gnomAD v3: 17-58281198-C-T
gnomAD v4: 17-58281198-C-T
MyVariant Identifiers: chr17:g.56358559C>T (hg19) chr17:g.58281198C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281198C>T , CM000679.2:g.58281198C>T GRCh38
NC_000017.10:g.56358559C>T , CM000679.1:g.56358559C>T GRCh37
NC_000017.9:g.53713558C>T NCBI36
NG_009629.1:g.4738G>A , LRG_84:g.4738G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-129G>A XP_011523123.1:n.71-129G>A
XM_011524823.1:c.71-129G>A XP_011523125.1:n.71-129G>A
Search 100 bp 5'
Search 100 bp 3'