Linked Data
gnomAD v4:
1-17394177-C-CAGG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17394178_17394180dup , CM000663.2:g.17394178_17394180dup | GRCh38 |
| NC_000001.10:g.17720674_17720676dup , CM000663.1:g.17720674_17720676dup | GRCh37 |
| NC_000001.9:g.17593261_17593263dup | NCBI36 |
| NG_032943.1:g.26933_26935dup | |
| NG_032943.2:g.26933_26935dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619609.1:c.1182+96_1182+98dup MANE Select | ENSP00000483125.1:n.1182+96_1182+98dup | |
| NM_207421.4:c.1182+96_1182+98dup MANE Select | NP_997304.3:n.1182+96_1182+98dup |