Canonical Allele Identifier: CA773487788
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1424414996
MyVariant Identifiers: chr17:g.56358482T>C (hg19) chr17:g.58281121T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281121T>C , CM000679.2:g.58281121T>C GRCh38
NC_000017.10:g.56358482T>C , CM000679.1:g.56358482T>C GRCh37
NC_000017.9:g.53713481T>C NCBI36
NG_009629.1:g.4815A>G , LRG_84:g.4815A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011524821.1:c.71-52A>G XP_011523123.1:n.71-52A>G
XM_011524823.1:c.71-52A>G XP_011523125.1:n.71-52A>G
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