Canonical Allele Identifier: CA122916
Gene: RAG1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13158
dbSNP Id: rs121918569

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36575637G>A , CM000673.2:g.36575637G>A GRCh38
NC_000011.8:g.36553763G>A NCBI36
NC_000011.9:g.36597187G>A , CM000673.1:g.36597187G>A GRCh37
NG_007528.1:g.12625G>A , LRG_98:g.12625G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299440.5:c.2333G>A ENSP00000299440.5:p.Arg778Gln
ENST00000524423.1:n.466C>T
ENST00000534663.1:c.2333G>A ENSP00000434610.1:p.Arg778Gln
NM_000448.2:c.2333G>A , LRG_98t1:c.2333G>A NP_000439.1:p.Arg778Gln
XM_005253041.3:c.2333G>A XP_005253098.1:p.Arg778Gln
XM_011520250.1:c.2333G>A XP_011518552.1:p.Arg778Gln
XM_011520251.1:c.2333G>A XP_011518553.1:p.Arg778Gln