Canonical Allele Identifier: CA438901764
Gene: SOD3 HGNC NCBI

Linked Data

dbSNP Id: rs1577363289
gnomAD v3: 4-24799731-G-A
gnomAD v4: 4-24799731-G-A
MyVariant Identifiers: chr4:g.24801353G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799731G>A , CM000666.2:g.24799731G>A GRCh38
NC_000004.11:g.24801353G>A , CM000666.1:g.24801353G>A GRCh37
NC_000004.10:g.24410451G>A NCBI36
NG_012213.1:g.9269G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.210G>A MANE Select ENSP00000371554.3:p.Thr70=
ENST00000382120.3:c.210G>A ENSP00000371554.3:p.Thr70=
NM_003102.2:c.210G>A NP_003093.2:p.Thr70=
XR_427488.1:n.400G>A
NM_003102.3:c.210G>A NP_003093.2:p.Thr70=
NM_003102.4:c.210G>A MANE Select NP_003093.2:p.Thr70=