Canonical Allele Identifier: CA356638905
Gene: SOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.24801394T>C (hg19) chr4:g.24799772T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799772T>C , CM000666.2:g.24799772T>C GRCh38
NC_000004.11:g.24801394T>C , CM000666.1:g.24801394T>C GRCh37
NC_000004.10:g.24410492T>C NCBI36
NG_012213.1:g.9310T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.251T>C MANE Select ENSP00000371554.3:p.Phe84Ser
ENST00000382120.3:c.251T>C ENSP00000371554.3:p.Phe84Ser
NM_003102.2:c.251T>C NP_003093.2:p.Phe84Ser
XR_427488.1:n.441T>C
NM_003102.3:c.251T>C NP_003093.2:p.Phe84Ser
NM_003102.4:c.251T>C MANE Select NP_003093.2:p.Phe84Ser
Search 100 bp 5'
Search 100 bp 3'