Canonical Allele Identifier: CA2580575813
Gene: SOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159693279G>A , CM000668.2:g.159693279G>A GRCh38
NC_000006.11:g.160114311G>A , CM000668.1:g.160114311G>A GRCh37
NC_000006.10:g.160034301G>A NCBI36
NG_008729.1:g.5043C>T
NG_008729.3:g.74251C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000401980.3:c.-115-416C>T ENSP00000384196.3:n.-115-416C>T
ENST00000535561.5:c.93-416C>T ENSP00000445015.1:n.93-416C>T
ENST00000537657.5:c.-115-416C>T ENSP00000439191.1:n.-115-416C>T
ENST00000538183.6:c.-112C>T ENSP00000446252.1:n.-112C>T
ENST00000545162.5:c.93-416C>T ENSP00000441362.1:n.93-416C>T
ENST00000546087.5:c.-115-416C>T ENSP00000442920.1:n.-115-416C>T
NM_000636.2:c.-112C>T NP_000627.2:n.-112C>T
NM_001024465.1:c.-112C>T NP_001019636.1:n.-112C>T
NM_001024466.1:c.-112C>T NP_001019637.1:n.-112C>T
NM_000636.3:c.-112C>T NP_000627.2:n.-112C>T
NM_001024465.2:c.-112C>T NP_001019636.1:n.-112C>T
NM_001024466.2:c.-112C>T NP_001019637.1:n.-112C>T
NM_001322814.1:c.-112C>T NP_001309743.1:n.-112C>T
NM_001322815.1:c.-112C>T NP_001309744.1:n.-112C>T
NM_001322816.1:c.-112C>T NP_001309745.1:n.-112C>T
NM_001322817.1:c.-115-416C>T NP_001309746.1:n.-115-416C>T
NM_001322819.1:c.-115-416C>T NP_001309748.1:n.-115-416C>T
NM_001322820.1:c.-115-416C>T NP_001309749.1:n.-115-416C>T
NM_001322817.2:c.-115-416C>T NP_001309746.1:n.-115-416C>T
NM_001322819.2:c.-115-416C>T NP_001309748.1:n.-115-416C>T
NM_001322820.2:c.-115-416C>T NP_001309749.1:n.-115-416C>T