Linked Data
gnomAD v4:
15-65077610-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077611del , CM000677.2:g.65077611del | GRCh38 |
| NC_000015.9:g.65369949del , CM000677.1:g.65369949del | GRCh37 |
| NC_000015.8:g.63157002del | NCBI36 |
| NG_021411.1:g.5796del , LRG_682:g.5796del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000432196.5:c.796del MANE Select | ENSP00000388723.2:p.Glu266AsnfsTer? | |
| ENST00000432196.3:c.796del | ENSP00000388723.2:p.Glu266AsnfsTer? | |
| NM_001101362.2:c.796del , LRG_682t1:c.796del | NP_001094832.1:p.Glu266AsnfsTer? | |
| NM_001101362.3:c.796del MANE Select | NP_001094832.1:p.Glu266AsnfsTer? |