Linked Data
gnomAD v4:
3-81649055-AGT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81649056_81649057del , CM000665.2:g.81649056_81649057del | GRCh38 |
| NC_000003.11:g.81698207_81698208del , CM000665.1:g.81698207_81698208del | GRCh37 |
| NC_000003.10:g.81780897_81780898del | NCBI36 |
| NG_011810.1:g.117744_117745del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.556-66_556-65del MANE Select | ENSP00000410833.2:n.556-66_556-65del | |
| ENST00000429644.6:c.556-66_556-65del | ENSP00000410833.2:n.556-66_556-65del | |
| ENST00000486920.1:n.552-66_552-65del | ||
| ENST00000489715.1:c.433-66_433-65del | ENSP00000419638.1:n.433-66_433-65del | |
| ENST00000498468.1:n.84-66_84-65del | ||
| NM_000158.3:c.556-66_556-65del | NP_000149.3:n.556-66_556-65del | |
| NM_000158.4:c.556-66_556-65del MANE Select | NP_000149.4:n.556-66_556-65del |