Linked Data
gnomAD v4:
10-114044060-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044063del , CM000672.2:g.114044063del | GRCh38 |
| NC_000010.10:g.115803822del , CM000672.1:g.115803822del | GRCh37 |
| NC_000010.9:g.115793812del | NCBI36 |
| NG_012187.1:g.5017del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.-70del MANE Select | ENSP00000358301.2:n.-70del | |
| ENST00000369295.3:c.-70del | ENSP00000358301.2:n.-70del | |
| NM_000684.2:c.-70del | NP_000675.1:n.-70del | |
| NM_000684.3:c.-70del MANE Select | NP_000675.1:n.-70del |