Canonical Allele Identifier: CA151102759
Gene: SOD2 HGNC NCBI

Linked Data

dbSNP Id: rs4516970

Genomic Alleles

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

Transcript Alleles

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