Linked Data
gnomAD v4:
15-42958177-A-AT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42958177_42958178insT , CM000677.2:g.42958177_42958178insT | GRCh38 |
| NC_000015.9:g.43250375_43250376insT , CM000677.1:g.43250375_43250376insT | GRCh37 |
| NC_000015.8:g.41037667_41037668insT | NCBI36 |
| NG_012182.1:g.152911_152912insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290650.9:c.4758-88_4758-87insA MANE Select | ENSP00000290650.4:n.4758-88_4758-87insA | |
| ENST00000290650.8:c.4758-88_4758-87insA | ENSP00000290650.4:n.4758-88_4758-87insA | |
| NM_174916.2:c.4758-88_4758-87insA | NP_777576.1:n.4758-88_4758-87insA | |
| NM_174916.3:c.4758-88_4758-87insA MANE Select | NP_777576.1:n.4758-88_4758-87insA |