Canonical Allele Identifier: CA400376840
Gene: MPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.56357755C>G (hg19) chr17:g.58280394C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280394C>G , CM000679.2:g.58280394C>G GRCh38
NC_000017.10:g.56357755C>G , CM000679.1:g.56357755C>G GRCh37
NC_000017.9:g.53712754C>G NCBI36
NG_009629.1:g.5542G>C , LRG_84:g.5542G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.220G>C MANE Select ENSP00000225275.3:p.Asp74His
ENST00000225275.3:c.220G>C ENSP00000225275.3:p.Asp74His
ENST00000580005.1:n.149G>C
NM_000250.1:c.220G>C , LRG_84t1:c.220G>C NP_000241.1:p.Asp74His
XM_011524821.1:c.406G>C XP_011523123.1:p.Asp136His
XM_011524822.1:c.-38+211G>C XP_011523124.1:n.-38+211G>C
XM_011524823.1:c.406G>C XP_011523125.1:p.Asp136His
NM_000250.2:c.220G>C MANE Select NP_000241.1:p.Asp74His
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