Linked Data
gnomAD v4:
21-45990482-A-AGAGATGTGCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990483_45990484insAGATGTGCCG , CM000683.2:g.45990483_45990484insAGATGTGCCG | GRCh38 |
| NC_000021.8:g.47410397_47410398insAGATGTGCCG , CM000683.1:g.47410397_47410398insAGATGTGCCG | GRCh37 |
| NC_000021.7:g.46234825_46234826insAGATGTGCCG | NCBI36 |
| NG_008674.1:g.13735_13736insAGATGTGCCG , LRG_475:g.13735_13736insAGATGTGCCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+61_1002+62insAGATGTGCCG MANE Select | ENSP00000355180.3:n.1002+61_1002+62insAGATGTGCCG | |
| ENST00000361866.7:c.1002+61_1002+62insAGATGTGCCG | ENSP00000355180.3:n.1002+61_1002+62insAGATGTGCCG | |
| ENST00000612273.1:c.1002+61_1002+62insAGATGTGCCG | ENSP00000483630.1:n.1002+61_1002+62insAGATGTGCCG | |
| NM_001848.2:c.1002+61_1002+62insAGATGTGCCG , LRG_475t1:c.1002+61_1002+62insAGATGTGCCG | NP_001839.2:n.1002+61_1002+62insAGATGTGCCG | |
| NM_001848.3:c.1002+61_1002+62insAGATGTGCCG MANE Select | NP_001839.2:n.1002+61_1002+62insAGATGTGCCG |