Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64756157C>A , CM000673.2:g.64756157C>A | GRCh38 |
| NC_000011.9:g.64523629C>A , CM000673.1:g.64523629C>A | GRCh37 |
| NC_000011.8:g.64280205C>A | NCBI36 |
| NG_013018.1:g.9559G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005609.4:c.661-599G>T MANE Select | NP_005600.1:n.661-599G>T |
| ENST00000164139.4:c.661-599G>T MANE Select | ENSP00000164139.3:n.661-599G>T |
| NM_001164716.1:c.397-599G>T | NP_001158188.1:n.397-599G>T |
| NM_005609.2:c.661-599G>T | NP_005600.1:n.661-599G>T |
| NM_005609.3:c.661-599G>T | NP_005600.1:n.661-599G>T |
| ENST00000164139.3:c.661-599G>T | ENSP00000164139.3:n.661-599G>T |
| ENST00000377432.7:c.397-599G>T | ENSP00000366650.3:n.397-599G>T |