Linked Data
gnomAD v4:
11-6319017-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319017C>T , CM000673.2:g.6319017C>T | GRCh38 |
| NC_000011.9:g.6340247C>T , CM000673.1:g.6340247C>T | GRCh37 |
| NC_000011.8:g.6296823C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*146G>A MANE Select | ENSP00000307292.3:n.*146G>A | |
| ENST00000303927.3:c.*146G>A | ENSP00000307292.3:n.*146G>A | |
| ENST00000532354.1:n.954G>A | ||
| NM_145040.2:c.*146G>A | NP_659477.2:n.*146G>A | |
| XR_930997.1:n.720+797C>T | ||
| NM_145040.3:c.*146G>A MANE Select | NP_659477.2:n.*146G>A |