Canonical Allele Identifier: CA512113688
Gene: SOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.33039547C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31667234C>T , CM000683.2:g.31667234C>T GRCh38
NC_000021.8:g.33039547C>T , CM000683.1:g.33039547C>T GRCh37
NC_000021.7:g.31961418C>T NCBI36
NG_008689.1:g.12613C>T , LRG_652:g.12613C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270142.11:c.240-24C>T MANE Select ENSP00000270142.7:n.240-24C>T
ENST00000270142.10:c.240-24C>T ENSP00000270142.6:n.240-24C>T
ENST00000389995.4:c.183-24C>T ENSP00000374645.4:n.183-24C>T
ENST00000470944.1:n.1168-24C>T
ENST00000476106.5:n.503-24C>T
NM_000454.4:c.240-24C>T , LRG_652t1:c.240-24C>T NP_000445.1:n.240-24C>T
NM_000454.5:c.240-24C>T MANE Select NP_000445.1:n.240-24C>T