Linked Data
gnomAD v4:
8-117835333-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117835334del , CM000670.2:g.117835334del | GRCh38 |
| NC_000008.10:g.118847573del , CM000670.1:g.118847573del | GRCh37 |
| NC_000008.9:g.118916754del | NCBI36 |
| NG_007455.2:g.281486del , LRG_493:g.281486del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.631+110del | ||
| ENST00000378204.7:c.1164+110del MANE Select | ENSP00000367446.3:n.1164+110del | |
| ENST00000436216.2:c.532+110del | ||
| ENST00000378204.6:c.1164+110del | ENSP00000367446.2:n.1164+110del | |
| ENST00000436216.1:c.532+110del | ||
| ENST00000437196.1:c.*55+110del | ENSP00000407299.1:n.*55+110del | |
| NM_000127.2:c.1164+110del , LRG_493t1:c.1164+110del | NP_000118.2:n.1164+110del | |
| NM_000127.3:c.1164+110del MANE Select | NP_000118.2:n.1164+110del |