Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216418513C>T , CM000663.2:g.216418513C>T | GRCh38 |
| NC_000001.10:g.216591855C>T , CM000663.1:g.216591855C>T | GRCh37 |
| NC_000001.9:g.214658478C>T | NCBI36 |
| NG_009497.1:g.9884G>A | |
| NG_009497.2:g.9936G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_206933.4:c.651+1G>A MANE Select | NP_996816.3:n.651+1G>A |
| ENST00000307340.8:c.651+1G>A MANE Select | ENSP00000305941.3:n.651+1G>A |
| NM_007123.5:c.651+1G>A | NP_009054.5:n.651+1G>A |
| NM_007123.6:c.651+1G>A | NP_009054.6:n.651+1G>A |
| NM_206933.2:c.651+1G>A | NP_996816.2:n.651+1G>A |
| NM_206933.3:c.651+1G>A | NP_996816.2:n.651+1G>A |
| ENST00000307340.7:c.651+1G>A | ENSP00000305941.3:n.651+1G>A |
| ENST00000366942.3:c.651+1G>A | ENSP00000355909.3:n.651+1G>A |
| ENST00000674083.1:c.651+1G>A | ENSP00000501296.1:n.651+1G>A |