Canonical Allele Identifier: CA292020219
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1034658403
MyVariant Identifiers: chr17:g.56358384T>A (hg19) chr17:g.58281023T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281023T>A , CM000679.2:g.58281023T>A GRCh38
NC_000017.10:g.56358384T>A , CM000679.1:g.56358384T>A GRCh37
NC_000017.9:g.53713383T>A NCBI36
NG_009629.1:g.4913A>T , LRG_84:g.4913A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.117A>T XP_011523123.1:p.Arg39Ser
XM_011524823.1:c.117A>T XP_011523125.1:p.Arg39Ser
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