Linked Data
gnomAD v4:
10-68231659-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231662del , CM000672.2:g.68231662del | GRCh38 |
| NC_000010.10:g.69991419del , CM000672.1:g.69991419del | GRCh37 |
| NC_000010.9:g.69661425del | NCBI36 |
| NG_031934.1:g.5454del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.18del MANE Select | ENSP00000362777.3:p.Ser7AlafsTer? | |
| ENST00000373673.4:c.18del | ENSP00000362777.3:p.Ser7AlafsTer? | |
| NM_145178.3:c.18del | NP_660161.1:p.Ser7AlafsTer? | |
| NM_145178.4:c.18del MANE Select | NP_660161.1:p.Ser7AlafsTer? |