Canonical Allele Identifier: CA292020659
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs984148024
MyVariant Identifiers: chr17:g.56358826C>A (hg19) chr17:g.58281465C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281465C>A , CM000679.2:g.58281465C>A GRCh38
NC_000017.10:g.56358826C>A , CM000679.1:g.56358826C>A GRCh37
NC_000017.9:g.53713825C>A NCBI36
NG_009629.1:g.4471G>T , LRG_84:g.4471G>T

Transcript Alleles

HGVS Amino-acid change
XM_011524821.1:c.71-396G>T XP_011523123.1:n.71-396G>T
XM_011524823.1:c.71-396G>T XP_011523125.1:n.71-396G>T
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