Linked Data
gnomAD v4:
15-97960944-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97960945dup , CM000677.2:g.97960945dup | GRCh38 |
| NC_000015.9:g.98504175dup , CM000677.1:g.98504175dup | GRCh37 |
| NC_000015.8:g.96305179dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268042.7:c.84dup MANE Select | ENSP00000268042.6:p.Lys29GlnfsTer? | |
| ENST00000268042.6:c.84dup | ENSP00000268042.6:p.Lys29GlnfsTer? | |
| NM_183376.2:c.84dup | NP_899232.2:p.Lys29GlnfsTer? | |
| NM_183376.3:c.84dup MANE Select | NP_899232.2:p.Lys29GlnfsTer? |