Linked Data
gnomAD v4:
10-114043995-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114043997del , CM000672.2:g.114043997del | GRCh38 |
| NC_000010.10:g.115803756del , CM000672.1:g.115803756del | GRCh37 |
| NC_000010.9:g.115793746del | NCBI36 |
| NG_012187.1:g.4951del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.-136del MANE Select | ENSP00000358301.2:n.-136del | |
| NM_000684.3:c.-136del MANE Select | NP_000675.1:n.-136del |