Canonical Allele Identifier: CA1676706379
Gene: SOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159677167G= , CM000668.2:g.159677167G= GRCh38
NC_000006.11:g.160098199G= , CM000668.1:g.160098199G= GRCh37
NC_000006.10:g.160018189G= NCBI36
NG_008729.1:g.21155C=
NG_008729.3:g.90363C=

Transcript Alleles

HGVS Amino-acid change
ENST00000538183.7:c.*5326C= MANE Select ENSP00000446252.1:n.*5326C=
ENST00000538183.6:c.*5326C= ENSP00000446252.1:n.*5326C=
NM_000636.4:c.*5326C= MANE Select NP_000627.2:n.*5326C=
NM_001322814.2:c.*5326C= NP_001309743.1:n.*5326C=
NM_001322815.2:c.*5326C= NP_001309744.1:n.*5326C=
NM_001322819.2:c.*5326C= NP_001309748.1:n.*5326C=
NM_001322820.2:c.*5326C= NP_001309749.1:n.*5326C=