Canonical Allele Identifier: CA15429124
Gene: SOD2 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159679084A>T , CM000668.2:g.159679084A>T GRCh38
NC_000006.11:g.160100116A>T , CM000668.1:g.160100116A>T GRCh37
NC_000006.10:g.160020106A>T NCBI36
NG_008729.1:g.19238T>A
NG_008729.3:g.88446T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000538183.7:c.*3409T>A MANE Select ENSP00000446252.1:n.*3409T>A
ENST00000367055.8:c.*234T>A ENSP00000356022.4:n.*234T>A
ENST00000538183.6:c.*3409T>A ENSP00000446252.1:n.*3409T>A
ENST00000546260.5:c.*3782T>A ENSP00000440131.1:n.*3782T>A
NM_000636.3:c.*3409T>A NP_000627.2:n.*3409T>A
NM_001024465.2:c.*234T>A NP_001019636.1:n.*234T>A
NM_001024466.2:c.*234T>A NP_001019637.1:n.*234T>A
NM_001322814.1:c.*3409T>A NP_001309743.1:n.*3409T>A
NM_001322815.1:c.*3409T>A NP_001309744.1:n.*3409T>A
NM_001322817.1:c.*234T>A NP_001309746.1:n.*234T>A
NM_001322819.1:c.*3409T>A NP_001309748.1:n.*3409T>A
NM_001322820.1:c.*3409T>A NP_001309749.1:n.*3409T>A
NM_000636.4:c.*3409T>A MANE Select NP_000627.2:n.*3409T>A
NM_001024465.3:c.*234T>A NP_001019636.1:n.*234T>A
NM_001024466.3:c.*234T>A NP_001019637.1:n.*234T>A
NM_001322814.2:c.*3409T>A NP_001309743.1:n.*3409T>A
NM_001322815.2:c.*3409T>A NP_001309744.1:n.*3409T>A
NM_001322817.2:c.*234T>A NP_001309746.1:n.*234T>A
NM_001322819.2:c.*3409T>A NP_001309748.1:n.*3409T>A
NM_001322820.2:c.*3409T>A NP_001309749.1:n.*3409T>A