Canonical Allele Identifier: CA438901966
Gene: SOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.24801476C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799854C>G , CM000666.2:g.24799854C>G GRCh38
NC_000004.11:g.24801476C>G , CM000666.1:g.24801476C>G GRCh37
NC_000004.10:g.24410574C>G NCBI36
NG_012213.1:g.9392C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.333C>G MANE Select ENSP00000371554.3:p.Arg111=
ENST00000382120.3:c.333C>G ENSP00000371554.3:p.Arg111=
NM_003102.2:c.333C>G NP_003093.2:p.Arg111=
XR_427488.1:n.523C>G
NM_003102.3:c.333C>G NP_003093.2:p.Arg111=
NM_003102.4:c.333C>G MANE Select NP_003093.2:p.Arg111=
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