Linked Data
gnomAD v4:
2-176093686-GA-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093690del , CM000664.2:g.176093690del | GRCh38 |
| NC_000002.11:g.176958418del , CM000664.1:g.176958418del | GRCh37 |
| NC_000002.10:g.176666664del | NCBI36 |
| NG_008137.1:g.5887del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392539.4:c.781+19del MANE Select | ENSP00000376322.3:n.781+19del | |
| ENST00000392539.3:c.781+19del | ENSP00000376322.3:n.781+19del | |
| NM_000523.3:c.781+19del | NP_000514.2:n.781+19del | |
| XM_011511068.1:c.725-790del | XP_011509370.1:n.725-790del | |
| XM_011511068.2:c.725-790del | XP_011509370.1:n.725-790del | |
| NM_000523.4:c.781+19del MANE Select | NP_000514.2:n.781+19del |