Canonical Allele Identifier: CA12255440

Gene: SOD2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159693540G>T , CM000668.2:g.159693540G>T	GRCh38
NC_000006.11:g.160114572G>T , CM000668.1:g.160114572G>T	GRCh37
NC_000006.10:g.160034562G>T	NCBI36
NG_008729.1:g.4782C>A
NG_008729.3:g.73990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401980.3:c.-115-677C>A	ENSP00000384196.3:n.-115-677C>A
ENST00000535561.5:c.93-677C>A	ENSP00000445015.1:n.93-677C>A
ENST00000537657.5:c.-115-677C>A	ENSP00000439191.1:n.-115-677C>A
ENST00000545162.5:c.93-677C>A	ENSP00000441362.1:n.93-677C>A
ENST00000546087.5:c.-115-677C>A	ENSP00000442920.1:n.-115-677C>A
NM_001322817.1:c.-115-677C>A	NP_001309746.1:n.-115-677C>A
NM_001322819.1:c.-115-677C>A	NP_001309748.1:n.-115-677C>A
NM_001322820.1:c.-115-677C>A	NP_001309749.1:n.-115-677C>A
NM_001322817.2:c.-115-677C>A	NP_001309746.1:n.-115-677C>A
NM_001322819.2:c.-115-677C>A	NP_001309748.1:n.-115-677C>A
NM_001322820.2:c.-115-677C>A	NP_001309749.1:n.-115-677C>A