Canonical Allele Identifier: CA748618744
Gene: SOD1 HGNC NCBI

Linked Data

dbSNP Id: rs1164835709
gnomAD v3: 21-31659866-T-C
gnomAD v4: 21-31659866-T-C
MyVariant Identifiers: chr21:g.33032179T>C (hg19) chr21:g.31659866T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31659866T>C , CM000683.2:g.31659866T>C GRCh38
NC_000021.8:g.33032179T>C , CM000683.1:g.33032179T>C GRCh37
NC_000021.7:g.31954050T>C NCBI36
NG_008689.1:g.5245T>C , LRG_652:g.5245T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270142.11:c.72+25T>C MANE Select ENSP00000270142.7:n.72+25T>C
ENST00000270142.10:c.72+25T>C ENSP00000270142.6:n.72+25T>C
ENST00000389995.4:c.15+82T>C ENSP00000374645.4:n.15+82T>C
ENST00000470944.1:n.158T>C
ENST00000476106.5:n.149+25T>C
NM_000454.4:c.72+25T>C , LRG_652t1:c.72+25T>C NP_000445.1:n.72+25T>C
NM_000454.5:c.72+25T>C MANE Select NP_000445.1:n.72+25T>C
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