Canonical Allele Identifier: CA2638975885
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280925C>A , CM000679.2:g.58280925C>A GRCh38
NC_000017.10:g.56358286C>A , CM000679.1:g.56358286C>A GRCh37
NC_000017.9:g.53713285C>A NCBI36
NG_009629.1:g.5011G>T , LRG_84:g.5011G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-167G>T MANE Select ENSP00000225275.3:n.-167G>T
ENST00000225275.3:c.-167G>T ENSP00000225275.3:n.-167G>T
NM_000250.1:c.-167G>T , LRG_84t1:c.-167G>T NP_000241.1:n.-167G>T
XM_011524821.1:c.215G>T XP_011523123.1:p.Arg72Ile
XM_011524823.1:c.215G>T XP_011523125.1:p.Arg72Ile
NM_000250.2:c.-167G>T MANE Select NP_000241.1:n.-167G>T