Linked Data
gnomAD v4:
15-73367792-T-TGCGCCGAG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367799_73367806dup , CM000677.2:g.73367799_73367806dup | GRCh38 |
| NC_000015.9:g.73660140_73660147dup , CM000677.1:g.73660140_73660147dup | GRCh37 |
| NC_000015.8:g.71447193_71447200dup | NCBI36 |
| NG_009063.1:g.6465_6472dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.471_478dup MANE Select | ENSP00000261917.3:p.Gln160ProfsTer? | |
| ENST00000261917.3:c.471_478dup | ENSP00000261917.3:p.Gln160ProfsTer? | |
| NM_005477.2:c.471_478dup | NP_005468.1:p.Gln160ProfsTer? | |
| NM_005477.3:c.471_478dup MANE Select | NP_005468.1:p.Gln160ProfsTer? |