Linked Data
gnomAD v4:
14-100882698-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100882698C>A , CM000676.2:g.100882698C>A | GRCh38 |
| NC_000014.8:g.101349035C>A , CM000676.1:g.101349035C>A | GRCh37 |
| NC_000014.7:g.100418788C>A | NCBI36 |
| NG_045001.1:g.7150G>T | |
| NG_045000.5:g.51430C>A | |
| NG_045000.6:g.51430C>A | |
| NG_045001.2:g.26025G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.2091G>T MANE Select | ENSP00000497482.1:p.Met697Ile | |
| ENST00000534062.1:c.2091G>T | ENSP00000435342.1:p.Met697Ile | |
| NM_001134888.2:c.2091G>T | NP_001128360.1:p.Met697Ile | |
| NM_001134888.3:c.2091G>T MANE Select | NP_001128360.1:p.Met697Ile |