Canonical Allele Identifier: CA292020682
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs966147983
gnomAD v3: 17-58281556-C-T
gnomAD v4: 17-58281556-C-T
MyVariant Identifiers: chr17:g.56358917C>T (hg19) chr17:g.58281556C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281556C>T , CM000679.2:g.58281556C>T GRCh38
NC_000017.10:g.56358917C>T , CM000679.1:g.56358917C>T GRCh37
NC_000017.9:g.53713916C>T NCBI36
NG_009629.1:g.4380G>A , LRG_84:g.4380G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-487G>A XP_011523123.1:n.71-487G>A
XM_011524823.1:c.71-487G>A XP_011523125.1:n.71-487G>A
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