Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.63559006G= , CM000672.2:g.63559006G= | GRCh38 |
| NC_000010.10:g.65318766G= , CM000672.1:g.65318766G= | GRCh37 |
| NC_000010.9:g.64988772G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001001330.3:c.33-7332G= MANE Select | NP_001001330.1:n.33-7332G= |
| ENST00000373758.5:c.33-7332G= MANE Select | ENSP00000362863.4:n.33-7332G= |
| NM_001001330.2:c.33-7332G= | NP_001001330.1:n.33-7332G= |
| ENST00000373758.4:c.33-7332G= | ENSP00000362863.4:n.33-7332G= |
| XM_011539501.1:c.33-7332G= | XP_011537803.1:n.33-7332G= |
| XM_011539501.2:c.33-7332G= | XP_011537803.1:n.33-7332G= |
| XM_017015896.1:c.33-7332G= | XP_016871385.1:n.33-7332G= |