Linked Data
gnomAD v4:
7-94401537-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94401538del , CM000669.2:g.94401538del | GRCh38 |
| NC_000007.13:g.94030850del , CM000669.1:g.94030850del | GRCh37 |
| NC_000007.12:g.93868786del | NCBI36 |
| NG_007405.1:g.11978del , LRG_2:g.11978del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.226-29del MANE Select | ENSP00000297268.6:n.226-29del | |
| ENST00000297268.10:c.226-29del | ENSP00000297268.6:n.226-29del | |
| ENST00000620463.1:c.220-29del | ENSP00000477719.1:n.220-29del | |
| NM_000089.3:c.226-29del , LRG_2t1:c.226-29del | NP_000080.2:n.226-29del | |
| NM_000089.4:c.226-29del MANE Select | NP_000080.2:n.226-29del |