Canonical Allele Identifier: CA438901771
Gene: SOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.24801356G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799734G>A , CM000666.2:g.24799734G>A GRCh38
NC_000004.11:g.24801356G>A , CM000666.1:g.24801356G>A GRCh37
NC_000004.10:g.24410454G>A NCBI36
NG_012213.1:g.9272G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.213G>A MANE Select ENSP00000371554.3:p.Leu71=
ENST00000382120.3:c.213G>A ENSP00000371554.3:p.Leu71=
NM_003102.2:c.213G>A NP_003093.2:p.Leu71=
XR_427488.1:n.403G>A
NM_003102.3:c.213G>A NP_003093.2:p.Leu71=
NM_003102.4:c.213G>A MANE Select NP_003093.2:p.Leu71=
Search 100 bp 5'
Search 100 bp 3'