Canonical Allele Identifier: CA356638921
Gene: SOD3 HGNC NCBI

Linked Data

gnomAD v4: 4-24799779-G-T
MyVariant Identifiers: chr4:g.24801401G>T (hg19) chr4:g.24799779G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799779G>T , CM000666.2:g.24799779G>T GRCh38
NC_000004.11:g.24801401G>T , CM000666.1:g.24801401G>T GRCh37
NC_000004.10:g.24410499G>T NCBI36
NG_012213.1:g.9317G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.258G>T MANE Select ENSP00000371554.3:p.Gln86His
ENST00000382120.3:c.258G>T ENSP00000371554.3:p.Gln86His
NM_003102.2:c.258G>T NP_003093.2:p.Gln86His
XR_427488.1:n.448G>T
NM_003102.3:c.258G>T NP_003093.2:p.Gln86His
NM_003102.4:c.258G>T MANE Select NP_003093.2:p.Gln86His
Search 100 bp 5'
Search 100 bp 3'