Canonical Allele Identifier: CA2267634660
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1970504885
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280516C>G , CM000679.2:g.58280516C>G GRCh38
NC_000017.10:g.56357877C>G , CM000679.1:g.56357877C>G GRCh37
NC_000017.9:g.53712876C>G NCBI36
NG_009629.1:g.5420G>C , LRG_84:g.5420G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.155-57G>C MANE Select ENSP00000225275.3:n.155-57G>C
ENST00000225275.3:c.155-57G>C ENSP00000225275.3:n.155-57G>C
ENST00000580005.1:n.84-57G>C
NM_000250.1:c.155-57G>C , LRG_84t1:c.155-57G>C NP_000241.1:n.155-57G>C
XM_011524821.1:c.341-57G>C XP_011523123.1:n.341-57G>C
XM_011524822.1:c.-38+89G>C XP_011523124.1:n.-38+89G>C
XM_011524823.1:c.341-57G>C XP_011523125.1:n.341-57G>C
NM_000250.2:c.155-57G>C MANE Select NP_000241.1:n.155-57G>C
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