Linked Data
gnomAD v4:
15-73367853-C-CG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367858dup , CM000677.2:g.73367858dup | GRCh38 |
| NC_000015.9:g.73660199dup , CM000677.1:g.73660199dup | GRCh37 |
| NC_000015.8:g.71447252dup | NCBI36 |
| NG_009063.1:g.6411dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.417dup MANE Select | ENSP00000261917.3:p.Gly140ArgfsTer? | |
| ENST00000261917.3:c.417dup | ENSP00000261917.3:p.Gly140ArgfsTer? | |
| NM_005477.2:c.417dup | NP_005468.1:p.Gly140ArgfsTer? | |
| NM_005477.3:c.417dup MANE Select | NP_005468.1:p.Gly140ArgfsTer? |