Canonical Allele Identifier: CA438901791
Gene: SOD3 HGNC NCBI

Linked Data

dbSNP Id: rs1052441151
MyVariant Identifiers: chr4:g.24801500G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.24799878G>C , CM000666.2:g.24799878G>C GRCh38
NC_000004.11:g.24801500G>C , CM000666.1:g.24801500G>C GRCh37
NC_000004.10:g.24410598G>C NCBI36
NG_012213.1:g.9416G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382120.4:c.357G>C MANE Select ENSP00000371554.3:p.Gly119=
ENST00000382120.3:c.357G>C ENSP00000371554.3:p.Gly119=
NM_003102.2:c.357G>C NP_003093.2:p.Gly119=
XR_427488.1:n.547G>C
NM_003102.3:c.357G>C NP_003093.2:p.Gly119=
NM_003102.4:c.357G>C MANE Select NP_003093.2:p.Gly119=