Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94413139A>G , CM000669.2:g.94413139A>G | GRCh38 |
| NC_000007.13:g.94042451A>G , CM000669.1:g.94042451A>G | GRCh37 |
| NC_000007.12:g.93880387A>G | NCBI36 |
| NG_007405.1:g.23579A>G , LRG_2:g.23579A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.1557+3A>G MANE Select | ENSP00000297268.6:n.1557+3A>G | |
| ENST00000297268.10:c.1557+3A>G | ENSP00000297268.6:n.1557+3A>G | |
| ENST00000620463.1:c.1551+3A>G | ENSP00000477719.1:n.1551+3A>G | |
| NM_000089.3:c.1557+3A>G , LRG_2t1:c.1557+3A>G | NP_000080.2:n.1557+3A>G | |
| NM_000089.4:c.1557+3A>G MANE Select | NP_000080.2:n.1557+3A>G |