Canonical Allele Identifier: CA292020570
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs990539791
MyVariant Identifiers: chr17:g.56358699_56358700del (hg19) chr17:g.58281338_58281339del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281339_58281340del , CM000679.2:g.58281339_58281340del GRCh38
NC_000017.10:g.56358700_56358701del , CM000679.1:g.56358700_56358701del GRCh37
NC_000017.9:g.53713699_53713700del NCBI36
NG_009629.1:g.4597_4598del , LRG_84:g.4597_4598del

Transcript Alleles

HGVS Amino-acid change
XM_011524821.1:c.71-270_71-269del XP_011523123.1:n.71-270_71-269del
XM_011524823.1:c.71-270_71-269del XP_011523125.1:n.71-270_71-269del
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