Linked Data
gnomAD v2:
15-73660194-CG-C
gnomAD v4:
15-73367853-CG-C
MyVariant Identifiers:
chr15:g.73660195del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367858del , CM000677.2:g.73367858del | GRCh38 |
| NC_000015.9:g.73660199del , CM000677.1:g.73660199del | GRCh37 |
| NC_000015.8:g.71447252del | NCBI36 |
| NG_009063.1:g.6411del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.417del MANE Select | ENSP00000261917.3:p.Gly140AlafsTer? | |
| ENST00000261917.3:c.417del | ENSP00000261917.3:p.Gly140AlafsTer? | |
| NM_005477.2:c.417del | NP_005468.1:p.Gly140AlafsTer? | |
| NM_005477.3:c.417del MANE Select | NP_005468.1:p.Gly140AlafsTer? |