Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.110460955T= , CM000673.2:g.110460955T= | GRCh38 |
| NC_000011.9:g.110331679T= , CM000673.1:g.110331679T= | GRCh37 |
| NC_000011.8:g.109836889T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260270.3:c.441-1399T= MANE Select | ENSP00000260270.2:n.441-1399T= | |
| ENST00000260270.2:c.441-1399T= | ENSP00000260270.2:n.441-1399T= | |
| NM_004109.4:c.441-1399T= | NP_004100.1:n.441-1399T= | |
| NM_004109.5:c.441-1399T= MANE Select | NP_004100.1:n.441-1399T= |