Canonical Allele Identifier: CA292020683
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs966147983
MyVariant Identifiers: chr17:g.58281556C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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