Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755259A>T , CM000677.2:g.74755259A>T | GRCh38 |
| NC_000015.9:g.75047600A>T , CM000677.1:g.75047600A>T | GRCh37 |
| NC_000015.8:g.72834653A>T | NCBI36 |
| NG_008431.1:g.37718A>T | |
| NG_008431.2:g.37718A>T | |
| NG_061543.1:g.11415A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*171A>T MANE Select | ENSP00000342007.4:n.*171A>T | |
| ENST00000343932.4:c.*171A>T | ENSP00000342007.4:n.*171A>T | |
| NM_000761.4:c.*171A>T | NP_000752.2:n.*171A>T | |
| NM_000761.5:c.*171A>T MANE Select | NP_000752.2:n.*171A>T |