Canonical Allele Identifier: CA438901979
Gene: SOD3 HGNC NCBI

Linked Data

dbSNP Id: rs1347155008
gnomAD v3: 4-24799971-G-C
gnomAD v4: 4-24799971-G-C
MyVariant Identifiers: chr4:g.24801593G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799971G>C , CM000666.2:g.24799971G>C GRCh38
NC_000004.11:g.24801593G>C , CM000666.1:g.24801593G>C GRCh37
NC_000004.10:g.24410691G>C NCBI36
NG_012213.1:g.9509G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.450G>C MANE Select ENSP00000371554.3:p.Ala150=
ENST00000382120.3:c.450G>C ENSP00000371554.3:p.Ala150=
NM_003102.2:c.450G>C NP_003093.2:p.Ala150=
XR_427488.1:n.640G>C
NM_003102.3:c.450G>C NP_003093.2:p.Ala150=
NM_003102.4:c.450G>C MANE Select NP_003093.2:p.Ala150=
Search 100 bp 5'
Search 100 bp 3'