Linked Data
gnomAD v4:
3-81705478-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81705482del , CM000665.2:g.81705482del | GRCh38 |
| NC_000003.11:g.81754633del , CM000665.1:g.81754633del | GRCh37 |
| NC_000003.10:g.81837323del | NCBI36 |
| NG_011810.1:g.61322del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.278del MANE Select | ENSP00000410833.2:p.Pro93ArgfsTer? | |
| ENST00000429644.6:c.278del | ENSP00000410833.2:p.Pro93ArgfsTer? | |
| ENST00000489715.1:c.155del | ENSP00000419638.1:p.Pro52ArgfsTer? | |
| NM_000158.3:c.278del | NP_000149.3:p.Pro93ArgfsTer? | |
| NM_000158.4:c.278del MANE Select | NP_000149.4:p.Pro93ArgfsTer? |