Canonical Allele Identifier: CA512111526
Gene: SOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.33036195A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31663882A>T , CM000683.2:g.31663882A>T GRCh38
NC_000021.8:g.33036195A>T , CM000683.1:g.33036195A>T GRCh37
NC_000021.7:g.31958066A>T NCBI36
NG_008689.1:g.9261A>T , LRG_652:g.9261A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270142.11:c.165A>T MANE Select ENSP00000270142.7:p.Thr55=
ENST00000270142.10:c.165A>T ENSP00000270142.6:p.Thr55=
ENST00000389995.4:c.108A>T ENSP00000374645.4:p.Thr36=
ENST00000470944.1:n.1093A>T
ENST00000476106.5:n.428A>T
NM_000454.4:c.165A>T , LRG_652t1:c.165A>T NP_000445.1:p.Thr55=
NM_000454.5:c.165A>T MANE Select NP_000445.1:p.Thr55=