Linked Data
gnomAD v4:
6-3154402-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154402T>C , CM000668.2:g.3154402T>C | GRCh38 |
| NC_000006.11:g.3154636T>C , CM000668.1:g.3154636T>C | GRCh37 |
| NC_000006.10:g.3099635T>C | NCBI36 |
| NG_042223.1:g.8148A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.799A>G MANE Select | ENSP00000369703.2:p.Met267Val | |
| ENST00000679400.1:n.855A>G | ||
| ENST00000679907.1:n.1187A>G | ||
| ENST00000680036.1:n.1581A>G | ||
| ENST00000680967.1:n.1889A>G | ||
| ENST00000333628.3:c.799A>G | ENSP00000369703.2:p.Met267Val | |
| NM_001069.2:c.799A>G | NP_001060.1:p.Met267Val | |
| NM_001310315.1:c.544A>G | NP_001297244.1:p.Met182Val | |
| NM_001069.3:c.799A>G MANE Select | NP_001060.1:p.Met267Val | |
| NM_001310315.2:c.544A>G | NP_001297244.1:p.Met182Val |