Linked Data
gnomAD v4:
9-136673640-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136673645del , CM000671.2:g.136673645del | GRCh38 |
| NC_000009.11:g.139568097del , CM000671.1:g.139568097del | GRCh37 |
| NC_000009.10:g.138687918del | NCBI36 |
| NG_008090.1:g.18819del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.*111del MANE Select | ENSP00000360761.2:n.*111del | |
| ENST00000371694.7:c.*111del | ENSP00000360759.3:n.*111del | |
| ENST00000371696.6:c.*111del | ENSP00000360761.2:n.*111del | |
| ENST00000538402.1:c.*111del | ENSP00000438919.1:n.*111del | |
| NM_001012727.1:c.*111del | NP_001012745.1:n.*111del | |
| NM_006412.3:c.*111del | NP_006403.2:n.*111del | |
| NM_006412.4:c.*111del MANE Select | NP_006403.2:n.*111del | |
| NM_001012727.2:c.*111del | NP_001012745.1:n.*111del |