Canonical Allele Identifier: CA292020536
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs922025817
MyVariant Identifiers: chr17:g.56358670G>A (hg19) chr17:g.58281309G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281309G>A , CM000679.2:g.58281309G>A GRCh38
NC_000017.10:g.56358670G>A , CM000679.1:g.56358670G>A GRCh37
NC_000017.9:g.53713669G>A NCBI36
NG_009629.1:g.4627C>T , LRG_84:g.4627C>T

Transcript Alleles

HGVS Amino-acid change
XM_011524821.1:c.71-240C>T XP_011523123.1:n.71-240C>T
XM_011524823.1:c.71-240C>T XP_011523125.1:n.71-240C>T
Search 100 bp 5'
Search 100 bp 3'