Canonical Allele Identifier: CA773487777
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs71365867
gnomAD v3: 17-58281120-C-CCT
gnomAD v4: 17-58281120-C-CCT
MyVariant Identifiers: chr17:g.56358481_56358482insCT (hg19) chr17:g.58281120_58281121insCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281120_58281121insCT , CM000679.2:g.58281120_58281121insCT GRCh38
NC_000017.10:g.56358481_56358482insCT , CM000679.1:g.56358481_56358482insCT GRCh37
NC_000017.9:g.53713480_53713481insCT NCBI36
NG_009629.1:g.4815_4816insAG , LRG_84:g.4815_4816insAG

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-52_71-51insAG XP_011523123.1:n.71-52_71-51insAG
XM_011524823.1:c.71-52_71-51insAG XP_011523125.1:n.71-52_71-51insAG
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