Linked Data
gnomAD v4:
12-21174727-A-AC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174727_21174728insC , CM000674.2:g.21174727_21174728insC | GRCh38 |
| NC_000012.11:g.21327661_21327662insC , CM000674.1:g.21327661_21327662insC | GRCh37 |
| NC_000012.10:g.21218928_21218929insC | NCBI36 |
| NG_011745.1:g.48534_48535insC , LRG_1022:g.48534_48535insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.359+18_359+19insC MANE Select | ENSP00000256958.2:n.359+18_359+19insC | |
| ENST00000256958.2:c.359+18_359+19insC | ENSP00000256958.2:n.359+18_359+19insC | |
| ENST00000543498.5:c.426-2049_426-2048insC | ||
| NM_006446.4:c.359+18_359+19insC , LRG_1022t1:c.359+18_359+19insC | NP_006437.3:n.359+18_359+19insC | |
| NM_006446.5:c.359+18_359+19insC MANE Select | NP_006437.3:n.359+18_359+19insC |