Canonical Allele Identifier: CA438901822
Gene: SOD3 HGNC NCBI

Linked Data

dbSNP Id: rs1713781081
gnomAD v3: 4-24799758-C-T
gnomAD v4: 4-24799758-C-T
MyVariant Identifiers: chr4:g.24801380C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799758C>T , CM000666.2:g.24799758C>T GRCh38
NC_000004.11:g.24801380C>T , CM000666.1:g.24801380C>T GRCh37
NC_000004.10:g.24410478C>T NCBI36
NG_012213.1:g.9296C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.237C>T MANE Select ENSP00000371554.3:p.Thr79=
ENST00000382120.3:c.237C>T ENSP00000371554.3:p.Thr79=
NM_003102.2:c.237C>T NP_003093.2:p.Thr79=
XR_427488.1:n.427C>T
NM_003102.3:c.237C>T NP_003093.2:p.Thr79=
NM_003102.4:c.237C>T MANE Select NP_003093.2:p.Thr79=
Search 100 bp 5'
Search 100 bp 3'