Canonical Allele Identifier: CA1676706333
Gene: SOD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159677060T= , CM000668.2:g.159677060T= GRCh38
NC_000006.11:g.160098092T= , CM000668.1:g.160098092T= GRCh37
NC_000006.10:g.160018082T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000538183.7:c.*5433A= MANE Select ENSP00000446252.1:n.*5433A=
ENST00000538183.6:c.*5433A= ENSP00000446252.1:n.*5433A=
NM_000636.4:c.*5433A= MANE Select NP_000627.2:n.*5433A=
NM_001322814.2:c.*5433A= NP_001309743.1:n.*5433A=
NM_001322815.2:c.*5433A= NP_001309744.1:n.*5433A=
NM_001322819.2:c.*5433A= NP_001309748.1:n.*5433A=
NM_001322820.2:c.*5433A= NP_001309749.1:n.*5433A=
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