Canonical Allele Identifier: CA1676706320
Gene: SOD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159677014G= , CM000668.2:g.159677014G= GRCh38
NC_000006.11:g.160098046G= , CM000668.1:g.160098046G= GRCh37
NC_000006.10:g.160018036G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000538183.7:c.*5479C= MANE Select ENSP00000446252.1:n.*5479C=
ENST00000538183.6:c.*5479C= ENSP00000446252.1:n.*5479C=
NM_000636.4:c.*5479C= MANE Select NP_000627.2:n.*5479C=
NM_001322814.2:c.*5479C= NP_001309743.1:n.*5479C=
NM_001322815.2:c.*5479C= NP_001309744.1:n.*5479C=
NM_001322819.2:c.*5479C= NP_001309748.1:n.*5479C=
NM_001322820.2:c.*5479C= NP_001309749.1:n.*5479C=
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