Canonical Allele Identifier: CA1676706347
Gene: SOD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159677081A= , CM000668.2:g.159677081A= GRCh38
NC_000006.11:g.160098113A= , CM000668.1:g.160098113A= GRCh37
NC_000006.10:g.160018103A= NCBI36
NG_008729.3:g.90449T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000538183.7:c.*5412T= MANE Select ENSP00000446252.1:n.*5412T=
ENST00000538183.6:c.*5412T= ENSP00000446252.1:n.*5412T=
NM_000636.4:c.*5412T= MANE Select NP_000627.2:n.*5412T=
NM_001322814.2:c.*5412T= NP_001309743.1:n.*5412T=
NM_001322815.2:c.*5412T= NP_001309744.1:n.*5412T=
NM_001322819.2:c.*5412T= NP_001309748.1:n.*5412T=
NM_001322820.2:c.*5412T= NP_001309749.1:n.*5412T=
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