Linked Data
gnomAD v4:
7-95324688-C-CTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.95324688_95324689insTT , CM000669.2:g.95324688_95324689insTT | GRCh38 |
| NC_000007.13:g.94954000_94954001insTT , CM000669.1:g.94954000_94954001insTT | GRCh37 |
| NC_000007.12:g.94791936_94791937insTT | NCBI36 |
| NG_008779.1:g.4884_4885insAA | |
| NG_008779.2:g.5018_5019insAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222381.7:c.-214_-213insAA | ENSP00000222381.3:n.-214_-213insAA | |
| NM_000446.6:c.-214_-213insAA | NP_000437.3:n.-214_-213insAA |