Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92613131G>T , CM000672.2:g.92613131G>T | GRCh38 |
| NC_000010.10:g.94372888G>T , CM000672.1:g.94372888G>T | GRCh37 |
| NC_000010.9:g.94362868G>T | NCBI36 |
| NG_032580.1:g.25064G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004523.4:c.789+1G>T MANE Select | NP_004514.2:n.789+1G>T |
| ENST00000260731.5:c.789+1G>T MANE Select | ENSP00000260731.3:n.789+1G>T |
| NM_004523.3:c.789+1G>T | NP_004514.2:n.789+1G>T |
| ENST00000260731.4:c.789+1G>T | ENSP00000260731.3:n.789+1G>T |
| ENST00000676621.1:c.789+1G>T | ENSP00000503639.1:n.789+1G>T |
| ENST00000676647.1:c.582+1G>T | ENSP00000503394.1:n.582+1G>T |
| ENST00000676757.1:c.582+1G>T | ENSP00000504289.1:n.582+1G>T |
| ENST00000677720.1:c.789+1G>T | ENSP00000504840.1:n.789+1G>T |