Canonical Allele Identifier: CA512113709
Gene: SOD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.33039555G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31667242G>C , CM000683.2:g.31667242G>C GRCh38
NC_000021.8:g.33039555G>C , CM000683.1:g.33039555G>C GRCh37
NC_000021.7:g.31961426G>C NCBI36
NG_008689.1:g.12621G>C , LRG_652:g.12621G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270142.11:c.240-16G>C MANE Select ENSP00000270142.7:n.240-16G>C
ENST00000270142.10:c.240-16G>C ENSP00000270142.6:n.240-16G>C
ENST00000389995.4:c.183-16G>C ENSP00000374645.4:n.183-16G>C
ENST00000470944.1:n.1168-16G>C
ENST00000476106.5:n.503-16G>C
NM_000454.4:c.240-16G>C , LRG_652t1:c.240-16G>C NP_000445.1:n.240-16G>C
NM_000454.5:c.240-16G>C MANE Select NP_000445.1:n.240-16G>C