Canonical Allele Identifier: CA9998954
Gene: SOD1 HGNC NCBI

Linked Data

dbSNP Id: rs369415073

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31667342A>G , CM000683.2:g.31667342A>G GRCh38
NC_000021.8:g.33039655A>G , CM000683.1:g.33039655A>G GRCh37
NC_000021.7:g.31961526A>G NCBI36
NG_008689.1:g.12721A>G , LRG_652:g.12721A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270142.11:c.324A>G MANE Select ENSP00000270142.7:p.Ser108=
ENST00000270142.10:c.324A>G ENSP00000270142.6:p.Ser108=
ENST00000389995.4:c.267A>G ENSP00000374645.4:p.Ser89=
ENST00000470944.1:n.1252A>G
NM_000454.4:c.324A>G , LRG_652t1:c.324A>G NP_000445.1:p.Ser108=
NM_000454.5:c.324A>G MANE Select NP_000445.1:p.Ser108=