Canonical Allele Identifier: CA366295804

Gene: SOD2

Linked Data

• MyVariant Identifiers: chr6:g.160113688C>G (hg19) ; chr6:g.159692656C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.159692656C>G , CM000668.2:g.159692656C>G	GRCh38
NC_000006.11:g.160113688C>G , CM000668.1:g.160113688C>G	GRCh37
NC_000006.10:g.160033678C>G	NCBI36
NG_008729.1:g.5666G>C
NG_008729.3:g.74874G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000538183.7:c.226+5G>C MANE Select	ENSP00000446252.1:n.226+5G>C
ENST00000337404.8:c.226+5G>C	ENSP00000337127.4:n.226+5G>C
ENST00000367054.6:c.226+5G>C	ENSP00000356021.2:n.226+5G>C
ENST00000367055.8:c.226+5G>C	ENSP00000356022.4:n.226+5G>C
ENST00000401980.3:c.88+5G>C	ENSP00000384196.3:n.88+5G>C
ENST00000444946.6:c.226+5G>C	ENSP00000404804.2:n.226+5G>C
ENST00000452684.2:c.231G>C	ENSP00000406713.2:p.Arg77Ser
ENST00000535561.5:c.295+5G>C	ENSP00000445015.1:n.295+5G>C
ENST00000537657.5:c.88+5G>C	ENSP00000439191.1:n.88+5G>C
ENST00000538183.6:c.226+5G>C	ENSP00000446252.1:n.226+5G>C
ENST00000545162.5:c.295+5G>C	ENSP00000441362.1:n.295+5G>C
ENST00000546087.5:c.88+5G>C	ENSP00000442920.1:n.88+5G>C
ENST00000546260.5:c.231G>C	ENSP00000440131.1:p.Arg77Ser
NM_000636.2:c.226+5G>C	NP_000627.2:n.226+5G>C
NM_001024465.1:c.226+5G>C	NP_001019636.1:n.226+5G>C
NM_001024466.1:c.226+5G>C	NP_001019637.1:n.226+5G>C
NM_000636.3:c.226+5G>C	NP_000627.2:n.226+5G>C
NM_001024465.2:c.226+5G>C	NP_001019636.1:n.226+5G>C
NM_001024466.2:c.226+5G>C	NP_001019637.1:n.226+5G>C
NM_001322814.1:c.226+5G>C	NP_001309743.1:n.226+5G>C
NM_001322815.1:c.226+5G>C	NP_001309744.1:n.226+5G>C
NM_001322816.1:c.231G>C	NP_001309745.1:p.Arg77Ser
NM_001322817.1:c.88+5G>C	NP_001309746.1:n.88+5G>C
NM_001322819.1:c.88+5G>C	NP_001309748.1:n.88+5G>C
NM_001322820.1:c.88+5G>C	NP_001309749.1:n.88+5G>C
NM_000636.4:c.226+5G>C MANE Select	NP_000627.2:n.226+5G>C
NM_001024465.3:c.226+5G>C	NP_001019636.1:n.226+5G>C
NM_001024466.3:c.226+5G>C	NP_001019637.1:n.226+5G>C
NM_001322814.2:c.226+5G>C	NP_001309743.1:n.226+5G>C
NM_001322815.2:c.226+5G>C	NP_001309744.1:n.226+5G>C
NM_001322817.2:c.88+5G>C	NP_001309746.1:n.88+5G>C
NM_001322819.2:c.88+5G>C	NP_001309748.1:n.88+5G>C
NM_001322820.2:c.88+5G>C	NP_001309749.1:n.88+5G>C
NM_001322816.2:c.231G>C	NP_001309745.1:p.Arg77Ser