Canonical Allele Identifier: CA438901921
Gene: SOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.24801431C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799809C>T , CM000666.2:g.24799809C>T GRCh38
NC_000004.11:g.24801431C>T , CM000666.1:g.24801431C>T GRCh37
NC_000004.10:g.24410529C>T NCBI36
NG_012213.1:g.9347C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.288C>T MANE Select ENSP00000371554.3:p.Phe96=
ENST00000382120.3:c.288C>T ENSP00000371554.3:p.Phe96=
NM_003102.2:c.288C>T NP_003093.2:p.Phe96=
XR_427488.1:n.478C>T
NM_003102.3:c.288C>T NP_003093.2:p.Phe96=
NM_003102.4:c.288C>T MANE Select NP_003093.2:p.Phe96=
Search 100 bp 5'
Search 100 bp 3'