Canonical Allele Identifier: CA2267634538
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs1970499005

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280271C>A , CM000679.2:g.58280271C>A GRCh38
NC_000017.10:g.56357632C>A , CM000679.1:g.56357632C>A GRCh37
NC_000017.9:g.53712631C>A NCBI36
NG_009629.1:g.5665G>T , LRG_84:g.5665G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.248+95G>T MANE Select ENSP00000225275.3:n.248+95G>T
ENST00000225275.3:c.248+95G>T ENSP00000225275.3:n.248+95G>T
ENST00000580005.1:n.259+13G>T
NM_000250.1:c.248+95G>T , LRG_84t1:c.248+95G>T NP_000241.1:n.248+95G>T
XM_011524821.1:c.434+95G>T XP_011523123.1:n.434+95G>T
XM_011524822.1:c.-37-257G>T XP_011523124.1:n.-37-257G>T
XM_011524823.1:c.434+95G>T XP_011523125.1:n.434+95G>T
NM_000250.2:c.248+95G>T MANE Select NP_000241.1:n.248+95G>T