Canonical Allele Identifier: CA773487791
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs71143240
gnomAD v3: 17-58281120-CTTT-C
gnomAD v4: 17-58281120-CTTT-C
MyVariant Identifiers: chr17:g.56358482_56358484del (hg19) chr17:g.58281121_58281123del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281136_58281138del , CM000679.2:g.58281136_58281138del GRCh38
NC_000017.10:g.56358497_56358499del , CM000679.1:g.56358497_56358499del GRCh37
NC_000017.9:g.53713496_53713498del NCBI36
NG_009629.1:g.4813_4815del , LRG_84:g.4813_4815del

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-54_71-52del XP_011523123.1:n.71-54_71-52del
XM_011524823.1:c.71-54_71-52del XP_011523125.1:n.71-54_71-52del
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