Canonical Allele Identifier: CA122919
Gene: RAG1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13159
ClinVar RCV Id: RCV000014045
dbSNP Id: rs121918570

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36576227C>T , CM000673.2:g.36576227C>T GRCh38
NC_000011.9:g.36597777C>T , CM000673.1:g.36597777C>T GRCh37
NC_000011.8:g.36554353C>T NCBI36
NG_007528.1:g.13215C>T , LRG_98:g.13215C>T

Transcript Alleles

HGVS Amino-acid change
NM_000448.2:c.2923C>T , LRG_98t1:c.2923C>T NP_000439.1:p.Arg975Trp
XM_005253041.3:c.2923C>T XP_005253098.1:p.Arg975Trp
XM_011520250.1:c.2923C>T XP_011518552.1:p.Arg975Trp
XM_011520251.1:c.2923C>T XP_011518553.1:p.Arg975Trp
XM_005253041.4:c.2923C>T XP_005253098.1:p.Arg975Trp
XM_011520250.2:c.2923C>T XP_011518552.1:p.Arg975Trp
ENST00000299440.5:c.2923C>T ENSP00000299440.5:p.Arg975Trp
ENST00000524423.1:n.132-256G>A
ENST00000534663.1:c.2789+134C>T ENSP00000434610.1:p.=