Canonical Allele Identifier: CA1676709853
Community Standard Title: NC_000006.12:g.159694389C=
Gene: SOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159694389C= , CM000668.2:g.159694389C= GRCh38
NC_000006.11:g.160115421C= , CM000668.1:g.160115421C= GRCh37
NC_000006.10:g.160035411C= NCBI36
NG_008729.1:g.3933G=
NG_008729.3:g.73141G=

Transcript Alleles

HGVS Amino-acid Change
NM_001322817.1:c.-115-1526G= NP_001309746.1:n.-115-1526G=
NM_001322817.2:c.-115-1526G= NP_001309746.1:n.-115-1526G=
NM_001322819.1:c.-115-1526G= NP_001309748.1:n.-115-1526G=
NM_001322819.2:c.-115-1526G= NP_001309748.1:n.-115-1526G=
NM_001322820.1:c.-115-1526G= NP_001309749.1:n.-115-1526G=
NM_001322820.2:c.-115-1526G= NP_001309749.1:n.-115-1526G=
ENST00000401980.3:c.-115-1526G= ENSP00000384196.3:n.-115-1526G=
ENST00000535561.5:c.93-1526G= ENSP00000445015.1:n.93-1526G=
ENST00000537657.5:c.-115-1526G= ENSP00000439191.1:n.-115-1526G=
ENST00000545162.5:c.93-1526G= ENSP00000441362.1:n.93-1526G=
ENST00000546087.5:c.-115-1526G= ENSP00000442920.1:n.-115-1526G=