Canonical Allele Identifier: CA410036830
Gene: SOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.33036196G>T (hg19) chr21:g.31663883G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31663883G>T , CM000683.2:g.31663883G>T GRCh38
NC_000021.8:g.33036196G>T , CM000683.1:g.33036196G>T GRCh37
NC_000021.7:g.31958067G>T NCBI36
NG_008689.1:g.9262G>T , LRG_652:g.9262G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270142.11:c.166G>T MANE Select ENSP00000270142.7:p.Ala56Ser
ENST00000270142.10:c.166G>T ENSP00000270142.6:p.Ala56Ser
ENST00000389995.4:c.109G>T ENSP00000374645.4:p.Ala37Ser
ENST00000470944.1:n.1094G>T
ENST00000476106.5:n.429G>T
NM_000454.4:c.166G>T , LRG_652t1:c.166G>T NP_000445.1:p.Ala56Ser
NM_000454.5:c.166G>T MANE Select NP_000445.1:p.Ala56Ser
Search 100 bp 5'
Search 100 bp 3'