Linked Data
gnomAD v4:
19-49060762-T-TTCTCA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49060764_49060768dup , CM000681.2:g.49060764_49060768dup | GRCh38 |
| NC_000019.9:g.49564021_49564025dup , CM000681.1:g.49564021_49564025dup | GRCh37 |
| NC_000019.8:g.54255833_54255837dup | NCBI36 |
| NG_016289.1:g.8101_8105dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000599795.5:c.243+988_243+992dup | ENSP00000470689.1:n.243+988_243+992dup | |
| XM_011527575.1:c.-15_-11dup | XP_011525877.1:n.-15_-11dup | |
| XR_001753693.1:n.879+397_879+401dup | ||
| XR_001753694.1:n.922_926dup |