Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.10982115A>G , CM000668.2:g.10982115A>G | GRCh38 |
| NC_000006.11:g.10982348A>G , CM000668.1:g.10982348A>G | GRCh37 |
| NC_000006.10:g.11090334A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354666.4:c.*1666T>C MANE Select | ENSP00000346693.3:n.*1666T>C | |
| ENST00000354666.3:c.*1666T>C | ENSP00000346693.3:n.*1666T>C | |
| NM_017770.3:c.*1666T>C | NP_060240.3:n.*1666T>C | |
| XM_011514716.1:c.*1666T>C | XP_011513018.1:n.*1666T>C | |
| XM_011514717.1:c.*1666T>C | XP_011513019.1:n.*1666T>C | |
| XM_011514716.3:c.*1666T>C | XP_011513018.1:n.*1666T>C | |
| NM_017770.4:c.*1666T>C MANE Select | NP_060240.3:n.*1666T>C |