Canonical Allele Identifier: CA292020678
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1007697871
gnomAD v3: 17-58281532-C-A
gnomAD v4: 17-58281532-C-A
MyVariant Identifiers: chr17:g.56358893C>A (hg19) chr17:g.58281532C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281532C>A , CM000679.2:g.58281532C>A GRCh38
NC_000017.10:g.56358893C>A , CM000679.1:g.56358893C>A GRCh37
NC_000017.9:g.53713892C>A NCBI36
NG_009629.1:g.4404G>T , LRG_84:g.4404G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-463G>T XP_011523123.1:n.71-463G>T
XM_011524823.1:c.71-463G>T XP_011523125.1:n.71-463G>T
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