Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.38363278C>T , CM000682.2:g.38363278C>T | GRCh38 |
| NC_000020.10:g.36991932C>T , CM000682.1:g.36991932C>T | GRCh37 |
| NC_000020.9:g.36425346C>T | NCBI36 |
| NG_034239.1:g.21868C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217407.3:c.653-697C>T MANE Select | ENSP00000217407.2:n.653-697C>T | |
| ENST00000217407.2:c.653-697C>T | ENSP00000217407.2:n.653-697C>T | |
| NM_004139.4:c.653-697C>T | NP_004130.2:n.653-697C>T | |
| NM_004139.5:c.653-697C>T MANE Select | NP_004130.2:n.653-697C>T |