Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92637571G>T , CM000672.2:g.92637571G>T | GRCh38 |
| NC_000010.10:g.94397328G>T , CM000672.1:g.94397328G>T | GRCh37 |
| NC_000010.9:g.94387308G>T | NCBI36 |
| NG_032580.1:g.49504G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2160+26G>T MANE Select | ENSP00000260731.3:n.2160+26G>T | |
| ENST00000676621.1:c.*678+26G>T | ENSP00000503639.1:n.*678+26G>T | |
| ENST00000676647.1:c.1953+26G>T | ENSP00000503394.1:n.1953+26G>T | |
| ENST00000676757.1:c.1953+26G>T | ENSP00000504289.1:n.1953+26G>T | |
| ENST00000677720.1:c.*134+26G>T | ENSP00000504840.1:n.*134+26G>T | |
| ENST00000260731.4:c.2160+26G>T | ENSP00000260731.3:n.2160+26G>T | |
| NM_004523.3:c.2160+26G>T | NP_004514.2:n.2160+26G>T | |
| NM_004523.4:c.2160+26G>T MANE Select | NP_004514.2:n.2160+26G>T |