Canonical Allele Identifier: CA1676721688
Gene: SOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.159716655G= , CM000668.2:g.159716655G= GRCh38
NC_000006.11:g.160137687G= , CM000668.1:g.160137687G= GRCh37
NC_000006.10:g.160057677G= NCBI36
NG_008729.3:g.50875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401980.3:c.-116+10474C= ENSP00000384196.3:n.-116+10474C=
ENST00000535561.5:c.92+10197C= ENSP00000445015.1:n.92+10197C=
ENST00000537657.5:c.-115-23792C= ENSP00000439191.1:n.-115-23792C=
ENST00000545162.5:c.92+10611C= ENSP00000441362.1:n.92+10611C=
ENST00000546087.5:c.-116+14230C= ENSP00000442920.1:n.-116+14230C=
NM_001322817.1:c.-116+14230C= NP_001309746.1:n.-116+14230C=
NM_001322819.1:c.-116+10611C= NP_001309748.1:n.-116+10611C=
NM_001322820.1:c.-116+10197C= NP_001309749.1:n.-116+10197C=
NM_001322817.2:c.-116+14230C= NP_001309746.1:n.-116+14230C=
NM_001322819.2:c.-116+10611C= NP_001309748.1:n.-116+10611C=
NM_001322820.2:c.-116+10197C= NP_001309749.1:n.-116+10197C=