Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46000778G>A , CM000683.2:g.46000778G>A | GRCh38 |
| NC_000021.8:g.47420692G>A , CM000683.1:g.47420692G>A | GRCh37 |
| NC_000021.7:g.46245120G>A | NCBI36 |
| NG_008674.1:g.24030G>A , LRG_475:g.24030G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.1822+11G>A MANE Select | NP_001839.2:n.1822+11G>A |
| ENST00000361866.8:c.1822+11G>A MANE Select | ENSP00000355180.3:n.1822+11G>A |
| NM_001848.2:c.1822+11G>A , LRG_475t1:c.1822+11G>A | NP_001839.2:n.1822+11G>A |
| ENST00000361866.7:c.1822+11G>A | ENSP00000355180.3:n.1822+11G>A |
| ENST00000466285.1:n.350G>A | |
| ENST00000612273.1:c.1816+408G>A | ENSP00000483630.1:n.1816+408G>A |