Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94962487G>A , CM000672.2:g.94962487G>A | GRCh38 |
| NC_000010.10:g.96722244G>A , CM000672.1:g.96722244G>A | GRCh37 |
| NC_000010.9:g.96712234G>A | NCBI36 |
| NG_008385.1:g.28830G>A | |
| NG_008385.2:g.29330G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000771.4:c.820-9617G>A MANE Select | NP_000762.2:n.820-9617G>A |
| ENST00000260682.8:c.820-9617G>A MANE Select | ENSP00000260682.6:n.820-9617G>A |
| NM_000771.3:c.820-9617G>A | NP_000762.2:n.820-9617G>A |
| ENST00000260682.6:c.820-9617G>A | ENSP00000260682.6:n.820-9617G>A |
| ENST00000643112.1:c.819+13203G>A | ENSP00000496202.1:n.819+13203G>A |