Canonical Allele Identifier: CA773487644
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1224366988
gnomAD v3: 17-58280934-T-A
gnomAD v4: 17-58280934-T-A
MyVariant Identifiers: chr17:g.56358295T>A (hg19) chr17:g.58280934T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280934T>A , CM000679.2:g.58280934T>A GRCh38
NC_000017.10:g.56358295T>A , CM000679.1:g.56358295T>A GRCh37
NC_000017.9:g.53713294T>A NCBI36
NG_009629.1:g.5002A>T , LRG_84:g.5002A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-176A>T MANE Select ENSP00000225275.3:n.-176A>T
ENST00000225275.3:c.-176A>T ENSP00000225275.3:n.-176A>T
NM_000250.1:c.-176A>T , LRG_84t1:c.-176A>T NP_000241.1:n.-176A>T
XM_011524821.1:c.206A>T XP_011523123.1:p.Asp69Val
XM_011524823.1:c.206A>T XP_011523125.1:p.Asp69Val
NM_000250.2:c.-176A>T MANE Select NP_000241.1:n.-176A>T
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