Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.120633145A>T , CM000665.2:g.120633145A>T | GRCh38 |
| NC_000003.11:g.120351992A>T , CM000665.1:g.120351992A>T | GRCh37 |
| NC_000003.10:g.121834682A>T | NCBI36 |
| NG_011957.1:g.54337T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000187.4:c.1188+2T>A MANE Select | NP_000178.2:n.1188+2T>A |
| ENST00000283871.10:c.1188+2T>A MANE Select | ENSP00000283871.5:n.1188+2T>A |
| NM_000187.3:c.1188+2T>A | NP_000178.2:n.1188+2T>A |
| ENST00000283871.9:c.1188+2T>A | ENSP00000283871.5:n.1188+2T>A |
| ENST00000492108.5:c.467+2T>A | ENSP00000419838.1:n.467+2T>A |
| XM_005247412.1:c.963+2T>A | XP_005247469.1:n.963+2T>A |
| XM_005247412.2:c.963+2T>A | XP_005247469.1:n.963+2T>A |
| XM_017006277.2:c.765+2T>A | XP_016861766.1:n.765+2T>A |