Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73483441G= , CM000666.2:g.73483441G= | GRCh38 |
| NC_000004.11:g.74349158G= , CM000666.1:g.74349158G= | GRCh37 |
| NC_000004.10:g.74568022G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226355.5:c.89-500G= MANE Select | ENSP00000226355.3:n.89-500G= | |
| ENST00000226355.4:c.89-500G= | ENSP00000226355.3:n.89-500G= | |
| NM_001133.2:c.89-500G= MANE Select | NP_001124.1:n.89-500G= | |
| XM_017007842.2:c.89-500G= | XP_016863331.1:n.89-500G= | |
| XM_017007843.2:c.89-500G= | XP_016863332.1:n.89-500G= | |
| XM_017007844.2:c.89-500G= | XP_016863333.1:n.89-500G= |