Linked Data
gnomAD v4:
15-73323203-AG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323206del , CM000677.2:g.73323206del | GRCh38 |
| NC_000015.9:g.73615547del , CM000677.1:g.73615547del | GRCh37 |
| NC_000015.8:g.71402600del | NCBI36 |
| NG_009063.1:g.51061del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.2889del MANE Select | ENSP00000261917.3:p.Ser964HisfsTer21 | |
| ENST00000261917.3:c.2889del | ENSP00000261917.3:p.Ser964HisfsTer21 | |
| NM_005477.2:c.2889del | NP_005468.1:p.Ser964HisfsTer21 | |
| XM_011521148.1:c.1671del | XP_011519450.1:p.Ser558HisfsTer21 | |
| XM_011521148.2:c.1671del | XP_011519450.1:p.Ser558HisfsTer21 | |
| NM_005477.3:c.2889del MANE Select | NP_005468.1:p.Ser964HisfsTer21 |