Linked Data
gnomAD v4:
11-6319026-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319026G>T , CM000673.2:g.6319026G>T | GRCh38 |
| NC_000011.9:g.6340256G>T , CM000673.1:g.6340256G>T | GRCh37 |
| NC_000011.8:g.6296832G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*137C>A MANE Select | ENSP00000307292.3:n.*137C>A | |
| ENST00000303927.3:c.*137C>A | ENSP00000307292.3:n.*137C>A | |
| ENST00000532354.1:n.945C>A | ||
| NM_145040.2:c.*137C>A | NP_659477.2:n.*137C>A | |
| XR_930997.1:n.720+806G>T | ||
| NM_145040.3:c.*137C>A MANE Select | NP_659477.2:n.*137C>A |