Linked Data
ClinVar Variation Id:
2942624
ClinVar RCV Id:
RCV003807790
dbSNP Id:
rs961233109
MyVariant Identifiers:
chr11:g.36597197G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.36575647G>A , CM000673.2:g.36575647G>A | GRCh38 |
| NC_000011.9:g.36597197G>A , CM000673.1:g.36597197G>A | GRCh37 |
| NC_000011.8:g.36553773G>A | NCBI36 |
| NG_007528.1:g.12635G>A , LRG_98:g.12635G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697713.1:c.2343G>A (RAG1) | ENSP00000513411.1:p.Gly781= | |
| ENST00000697714.1:c.2343G>A (RAG1) | ENSP00000513412.1:p.Gly781= | |
| ENST00000697715.1:c.2343G>A (RAG1) | ENSP00000513413.1:p.Gly781= | |
| ENST00000299440.6:c.2343G>A (RAG1) MANE Select | ENSP00000299440.5:p.Gly781= | |
| ENST00000299440.5:c.2343G>A (RAG1) | ENSP00000299440.5:p.Gly781= | |
| ENST00000524423.1:n.456C>T (RAG2) | ||
| ENST00000534663.1:c.2343G>A (RAG1) | ENSP00000434610.1:p.Gly781= | |
| NM_000448.2:c.2343G>A , LRG_98t1:c.2343G>A (RAG1) | NP_000439.1:p.Gly781= | |
| XM_005253041.3:c.2343G>A (RAG1) | XP_005253098.1:p.Gly781= | |
| XM_011520250.1:c.2343G>A (RAG1) | XP_011518552.1:p.Gly781= | |
| XM_011520251.1:c.2343G>A (RAG1) | XP_011518553.1:p.Gly781= | |
| XM_005253041.4:c.2343G>A (RAG1) | XP_005253098.1:p.Gly781= | |
| XM_011520250.2:c.2343G>A (RAG1) | XP_011518552.1:p.Gly781= | |
| NM_000448.3:c.2343G>A (RAG1) MANE Select | NP_000439.2:p.Gly781= | |
| NM_001377277.1:c.2343G>A (RAG1) | NP_001364206.1:p.Gly781= | |
| NM_001377278.1:c.2343G>A (RAG1) | NP_001364207.1:p.Gly781= | |
| NM_001377279.1:c.2343G>A (RAG1) | NP_001364208.1:p.Gly781= | |
| NM_001377280.1:c.2343G>A (RAG1) | NP_001364209.1:p.Gly781= |