Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155290151C>T , CM000663.2:g.155290151C>T | GRCh38 |
| NC_000001.10:g.155259942C>T , CM000663.1:g.155259942C>T | GRCh37 |
| NC_000001.9:g.153526566C>T | NCBI36 |
| NG_011677.1:g.16284G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342741.6:c.*421G>A MANE Select | ENSP00000339933.4:n.*421G>A | |
| ENST00000392414.7:c.*421G>A | ENSP00000376214.3:n.*421G>A | |
| NM_000298.5:c.*421G>A | NP_000289.1:n.*421G>A | |
| NM_181871.3:c.*421G>A | NP_870986.1:n.*421G>A | |
| NM_000298.6:c.*421G>A MANE Select | NP_000289.1:n.*421G>A | |
| NM_181871.4:c.*421G>A | NP_870986.1:n.*421G>A |