Canonical Allele Identifier: CA985008547
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1970516914
gnomAD v3: 17-58281217-T-C
gnomAD v4: 17-58281217-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58281217T>C , CM000679.2:g.58281217T>C GRCh38
NC_000017.10:g.56358578T>C , CM000679.1:g.56358578T>C GRCh37
NC_000017.9:g.53713577T>C NCBI36
NG_009629.1:g.4719A>G , LRG_84:g.4719A>G

Transcript Alleles

HGVS Amino-acid change
XM_011524821.1:c.71-148A>G XP_011523123.1:n.71-148A>G
XM_011524823.1:c.71-148A>G XP_011523125.1:n.71-148A>G
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