Linked Data
gnomAD v4:
8-19967125-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19967128del , CM000670.2:g.19967128del | GRCh38 |
| NC_000008.10:g.19824639del , CM000670.1:g.19824639del | GRCh37 |
| NC_000008.9:g.19868919del | NCBI36 |
| NG_008855.1:g.33058del | |
| NG_008855.2:g.70412del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.*1818del MANE Select | ENSP00000497642.1:n.*1818del | |
| ENST00000650478.1:c.2186del | ENSP00000497560.1:n.2186del | |
| ENST00000311322.8:c.*1818del | ENSP00000309757.6:n.*1818del | |
| NM_000237.2:c.*1818del | NP_000228.1:n.*1818del | |
| NM_000237.3:c.*1818del MANE Select | NP_000228.1:n.*1818del |