Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.76727669A= , CM000667.2:g.76727669A= | GRCh38 |
| NC_000005.9:g.76023494A= , CM000667.1:g.76023494A= | GRCh37 |
| NC_000005.8:g.76059250A= | NCBI36 |
| NG_032906.1:g.16627A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001992.5:c.89-4645A= MANE Select | NP_001983.2:n.89-4645A= |
| ENST00000319211.5:c.89-4645A= MANE Select | ENSP00000321326.4:n.89-4645A= |
| NM_001311313.1:c.-397-1043A= | NP_001298242.1:n.-397-1043A= |
| NM_001311313.2:c.-397-1043A= | NP_001298242.1:n.-397-1043A= |
| NM_001992.3:c.89-4645A= | NP_001983.2:n.89-4645A= |
| NM_001992.4:c.89-4645A= | NP_001983.2:n.89-4645A= |
| ENST00000319211.4:c.89-4645A= | ENSP00000321326.4:n.89-4645A= |