Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213812T= , CM000667.2:g.1213812T= | GRCh38 |
| NC_000005.9:g.1213927T= , CM000667.1:g.1213927T= | GRCh37 |
| NC_000005.8:g.1266927T= | NCBI36 |
| NG_008282.1:g.17218T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.775-141T= MANE Select | ENSP00000305302.10:n.775-141T= | |
| ENST00000304460.10:c.775-141T= | ENSP00000305302.10:n.775-141T= | |
| ENST00000515652.5:c.683-141T= | ENSP00000425701.1:n.683-141T= | |
| NM_001003841.2:c.775-141T= | NP_001003841.1:n.775-141T= | |
| NM_001003841.3:c.775-141T= MANE Select | NP_001003841.1:n.775-141T= |