Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65949728A= , CM000674.2:g.65949728A= | GRCh38 |
| NC_000012.11:g.66343508A= , CM000674.1:g.66343508A= | GRCh37 |
| NC_000012.10:g.64629775A= | NCBI36 |
| NG_016296.1:g.130269A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403681.7:c.250-1655A= MANE Select | ENSP00000384026.2:n.250-1655A= | |
| ENST00000393577.7:c.250-1655A= | ENSP00000377205.3:n.250-1655A= | |
| ENST00000403681.6:c.250-1655A= | ENSP00000384026.2:n.250-1655A= | |
| ENST00000539662.1:c.287-1655A= | ENSP00000440919.1:n.287-1655A= | |
| ENST00000541363.5:c.250-1655A= | ENSP00000439317.1:n.250-1655A= | |
| NM_001300918.1:c.250-1655A= | NP_001287847.1:n.250-1655A= | |
| NM_003483.4:c.250-1655A= | NP_003474.1:n.250-1655A= | |
| NM_003483.6:c.250-1655A= MANE Select | NP_003474.1:n.250-1655A= |