Linked Data
gnomAD v4:
11-6318987-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6318987T>G , CM000673.2:g.6318987T>G | GRCh38 |
| NC_000011.9:g.6340217T>G , CM000673.1:g.6340217T>G | GRCh37 |
| NC_000011.8:g.6296793T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*176A>C MANE Select | ENSP00000307292.3:n.*176A>C | |
| ENST00000303927.3:c.*176A>C | ENSP00000307292.3:n.*176A>C | |
| ENST00000532354.1:n.984A>C | ||
| NM_145040.2:c.*176A>C | NP_659477.2:n.*176A>C | |
| XR_930997.1:n.720+767T>G | ||
| NM_145040.3:c.*176A>C MANE Select | NP_659477.2:n.*176A>C |