Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46003811C>G , CM000683.2:g.46003811C>G | GRCh38 |
| NC_000021.8:g.47423725C>G , CM000683.1:g.47423725C>G | GRCh37 |
| NC_000021.7:g.46248153C>G | NCBI36 |
| NG_008674.1:g.27063C>G , LRG_475:g.27063C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.2885C>G MANE Select | NP_001839.2:p.Ala962Gly |
| ENST00000361866.8:c.2885C>G MANE Select | ENSP00000355180.3:p.Ala962Gly |
| NM_001848.2:c.2885C>G , LRG_475t1:c.2885C>G | NP_001839.2:p.Ala962Gly |
| ENST00000361866.7:c.2885C>G | ENSP00000355180.3:p.Ala962Gly |
| ENST00000463060.6:n.1284C>G | |
| ENST00000486023.1:n.673C>G | |
| ENST00000498614.5:n.1119C>G | |
| ENST00000612273.1:c.2879C>G | ENSP00000483630.1:p.Ala960Gly |
| ENST00000612273.2:c.1011C>G | |
| ENST00000682634.1:c.1011C>G |