Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94424688T= , CM000669.2:g.94424688T= | GRCh38 |
| NC_000007.13:g.94054000T= , CM000669.1:g.94054000T= | GRCh37 |
| NC_000007.12:g.93891936T= | NCBI36 |
| NG_007405.1:g.35128T= , LRG_2:g.35128T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2673+245T= MANE Select | NP_000080.2:n.2673+245T= |
| ENST00000297268.11:c.2673+245T= MANE Select | ENSP00000297268.6:n.2673+245T= |
| NM_000089.3:c.2673+245T= , LRG_2t1:c.2673+245T= | NP_000080.2:n.2673+245T= |
| ENST00000297268.10:c.2673+245T= | ENSP00000297268.6:n.2673+245T= |
| ENST00000469732.1:n.456+245T= | |
| ENST00000481570.5:n.2218T= | |
| ENST00000620463.1:c.2667+245T= | ENSP00000477719.1:n.2667+245T= |