Linked Data
gnomAD v4:
6-24178208-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24178208C>G , CM000668.2:g.24178208C>G | GRCh38 |
| NC_000006.11:g.24178436C>G , CM000668.1:g.24178436C>G | GRCh37 |
| NC_000006.10:g.24286415C>G | NCBI36 |
| NG_012829.1:g.184845G>C | |
| NG_012829.2:g.210085G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.1326+122G>C MANE Select | ENSP00000367715.3:n.1326+122G>C | |
| ENST00000378450.6:c.585+122G>C | ENSP00000367711.3:n.585+122G>C | |
| ENST00000378454.7:c.1326+122G>C | ENSP00000367715.3:n.1326+122G>C | |
| NM_001195610.1:c.1326+122G>C | NP_001182539.1:n.1326+122G>C | |
| NM_016356.4:c.1326+122G>C | NP_057440.2:n.1326+122G>C | |
| NM_016356.5:c.1326+122G>C MANE Select | NP_057440.2:n.1326+122G>C | |
| NM_001195610.2:c.1326+122G>C | NP_001182539.1:n.1326+122G>C |