Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.94935422T= , CM000666.2:g.94935422T= | GRCh38 |
| NC_000004.11:g.95856573T= , CM000666.1:g.95856573T= | GRCh37 |
| NC_000004.10:g.96075596T= | NCBI36 |
| NG_009245.1:g.182446T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515059.6:c.-113+59522T= MANE Select | ENSP00000426617.1:n.-113+59522T= | |
| ENST00000515059.5:c.-113+59522T= | ENSP00000426617.1:n.-113+59522T= | |
| NM_001203.2:c.-113+59522T= | NP_001194.1:n.-113+59522T= | |
| XM_011532201.1:c.-18+59522T= | XP_011530503.1:n.-18+59522T= | |
| XM_011532201.2:c.-18+59522T= | XP_011530503.1:n.-18+59522T= | |
| XM_017008558.1:c.-113+59522T= | XP_016864047.1:n.-113+59522T= | |
| XM_017008559.1:c.-113+36372T= | XP_016864048.1:n.-113+36372T= | |
| NM_001203.3:c.-113+59522T= MANE Select | NP_001194.1:n.-113+59522T= |