Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97960850T= , CM000677.2:g.97960850T= | GRCh38 |
| NC_000015.9:g.98504080T= , CM000677.1:g.98504080T= | GRCh37 |
| NC_000015.8:g.96305084T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268042.7:c.-12T= MANE Select | ENSP00000268042.6:n.-12T= | |
| ENST00000268042.6:c.-12T= | ENSP00000268042.6:n.-12T= | |
| NM_183376.2:c.-12T= | NP_899232.2:n.-12T= | |
| NM_183376.3:c.-12T= MANE Select | NP_899232.2:n.-12T= |