Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541823C>G , CM000663.2:g.169541823C>G | GRCh38 |
| NC_000001.10:g.169511061C>G , CM000663.1:g.169511061C>G | GRCh37 |
| NC_000001.9:g.167777685C>G | NCBI36 |
| NG_011806.1:g.49709G>C , LRG_553:g.49709G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.3267G>C MANE Select | ENSP00000356771.3:p.Met1089Ile | |
| ENST00000367796.3:c.3282G>C | ENSP00000356770.3:p.Met1094Ile | |
| ENST00000367797.7:c.3267G>C | ENSP00000356771.3:p.Met1089Ile | |
| NM_000130.4:c.3267G>C , LRG_553t1:c.3267G>C | NP_000121.2:p.Met1089Ile | |
| XM_017000660.2:c.2856G>C | XP_016856149.1:p.Met952Ile | |
| NM_000130.5:c.3267G>C MANE Select | NP_000121.2:p.Met1089Ile |