Linked Data
gnomAD v4:
22-20888367-CATTAT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20888368_20888372del , CM000684.2:g.20888368_20888372del | GRCh38 |
| NC_000022.10:g.21242656_21242660del , CM000684.1:g.21242656_21242660del | GRCh37 |
| NC_000022.9:g.19572656_19572660del | NCBI36 |
| NG_012152.1:g.34365_34369del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215730.12:c.*532_*536del MANE Select | ENSP00000215730.6:n.*532_*536del | |
| ENST00000215730.11:c.*532_*536del | ENSP00000215730.6:n.*532_*536del | |
| NM_004782.3:c.*532_*536del | NP_004773.1:n.*532_*536del | |
| NM_004782.4:c.*532_*536del MANE Select | NP_004773.1:n.*532_*536del |