Canonical Allele Identifier: CA292020767
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs753187124
gnomAD v3: 17-58281705-T-C
gnomAD v4: 17-58281705-T-C
MyVariant Identifiers: chr17:g.56359066T>C (hg19) chr17:g.58281705T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281705T>C , CM000679.2:g.58281705T>C GRCh38
NC_000017.10:g.56359066T>C , CM000679.1:g.56359066T>C GRCh37
NC_000017.9:g.53714065T>C NCBI36
NG_009629.1:g.4231A>G , LRG_84:g.4231A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-636A>G XP_011523123.1:n.71-636A>G
XM_011524823.1:c.71-636A>G XP_011523125.1:n.71-636A>G
Search 100 bp 5'
Search 100 bp 3'