Canonical Allele Identifier: CA292020131
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1054487240
gnomAD v3: 17-58280937-G-A
gnomAD v4: 17-58280937-G-A
MyVariant Identifiers: chr17:g.56358298G>A (hg19) chr17:g.58280937G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280937G>A , CM000679.2:g.58280937G>A GRCh38
NC_000017.10:g.56358298G>A , CM000679.1:g.56358298G>A GRCh37
NC_000017.9:g.53713297G>A NCBI36
NG_009629.1:g.4999C>T , LRG_84:g.4999C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.203C>T XP_011523123.1:p.Ala68Val
XM_011524823.1:c.203C>T XP_011523125.1:p.Ala68Val
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