Linked Data
dbSNP Id:
rs2102734822
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431393_229431394insCT , CM000663.2:g.229431393_229431394insCT | GRCh38 |
| NC_000001.10:g.229567140_229567141insCT , CM000663.1:g.229567140_229567141insCT | GRCh37 |
| NC_000001.9:g.227633763_227633764insCT | NCBI36 |
| NG_006672.1:g.7703_7704insAG , LRG_429:g.7703_7704insAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.*105_*106insAG | ENSP00000355644.4:n.*105_*106insAG | |
| ENST00000684723.1:c.*105_*106insAG | ENSP00000508084.1:n.*105_*106insAG | |
| ENST00000366683.3:c.*105_*106insAG | ENSP00000355644.3:n.*105_*106insAG | |
| ENST00000366684.7:c.*105_*106insAG MANE Select | ENSP00000355645.3:n.*105_*106insAG | |
| NM_001100.3:c.*105_*106insAG , LRG_429t1:c.*105_*106insAG | NP_001091.1:n.*105_*106insAG | |
| NM_001100.4:c.*105_*106insAG MANE Select | NP_001091.1:n.*105_*106insAG |