Canonical Allele Identifier: CA438901667
Gene: SOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.24801302G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799680G>A , CM000666.2:g.24799680G>A GRCh38
NC_000004.11:g.24801302G>A , CM000666.1:g.24801302G>A GRCh37
NC_000004.10:g.24410400G>A NCBI36
NG_012213.1:g.9218G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.159G>A MANE Select ENSP00000371554.3:p.Arg53=
ENST00000382120.3:c.159G>A ENSP00000371554.3:p.Arg53=
ENST00000598411.1:c.159G>A ENSP00000472134.1:p.Arg53=
NM_003102.2:c.159G>A NP_003093.2:p.Arg53=
XR_427488.1:n.349G>A
NM_003102.3:c.159G>A NP_003093.2:p.Arg53=
NM_003102.4:c.159G>A MANE Select NP_003093.2:p.Arg53=