Linked Data
gnomAD v4:
22-39244801-CTTTTTTT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.39244811_39244817del , CM000684.2:g.39244811_39244817del | GRCh38 |
| NC_000022.10:g.39640816_39640822del , CM000684.1:g.39640816_39640822del | GRCh37 |
| NC_000022.9:g.37970762_37970768del | NCBI36 |
| NG_012111.1:g.5145_5151del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331163.11:c.-845_-839del MANE Select | ENSP00000330382.6:n.-845_-839del | |
| NM_002608.2:c.-845_-839del | NP_002599.1:n.-845_-839del | |
| NM_002608.3:c.-845_-839del | NP_002599.1:n.-845_-839del | |
| NM_002608.4:c.-845_-839del MANE Select | NP_002599.1:n.-845_-839del |