Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46085701T= , CM000666.2:g.46085701T= | GRCh38 |
| NC_000004.11:g.46087718T= , CM000666.1:g.46087718T= | GRCh37 |
| NC_000004.10:g.45782475T= | NCBI36 |
| NG_046964.1:g.43365A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295452.5:c.254-1648A= MANE Select | ENSP00000295452.4:n.254-1648A= | |
| ENST00000295452.4:c.254-1648A= | ENSP00000295452.4:n.254-1648A= | |
| NM_173536.3:c.254-1648A= | NP_775807.2:n.254-1648A= | |
| NM_173536.4:c.254-1648A= MANE Select | NP_775807.2:n.254-1648A= |