Linked Data
gnomAD v4:
22-17084988-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.17084991del , CM000684.2:g.17084991del | GRCh38 |
| NC_000022.10:g.17565881del , CM000684.1:g.17565881del | GRCh37 |
| NC_000022.9:g.15945881del | NCBI36 |
| NG_028257.1:g.5031del , LRG_355:g.5031del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319363.10:c.-101del | ENSP00000320936.6:n.-101del | |
| ENST00000477874.1:n.38del | ||
| ENST00000612619.1:c.-101del | ENSP00000479970.1:n.-101del | |
| NM_001289905.1:c.-101del | NP_001276834.1:n.-101del | |
| NM_014339.6:c.-101del , LRG_355t1:c.-101del | NP_055154.3:n.-101del |