Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55063691G>T , CM000663.2:g.55063691G>T | GRCh38 |
| NC_000001.10:g.55529364G>T , CM000663.1:g.55529364G>T | GRCh37 |
| NC_000001.9:g.55301952G>T | NCBI36 |
| NG_009061.1:g.29145G>T , LRG_275:g.29145G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.*526G>T | ENSP00000501161.2:n.*526G>T | |
| ENST00000710286.1:c.*107G>T | ENSP00000518176.1:n.*107G>T | |
| ENST00000673903.1:c.*107G>T | ENSP00000501257.1:n.*107G>T | |
| ENST00000302118.5:c.*107G>T MANE Select | ENSP00000303208.5:n.*107G>T | |
| ENST00000490692.1:n.2732G>T | ||
| NM_174936.3:c.*107G>T , LRG_275t1:c.*107G>T | NP_777596.2:n.*107G>T | |
| NR_110451.1:n.1793G>T | ||
| XM_011541193.1:c.*107G>T | XP_011539495.1:n.*107G>T | |
| NM_174936.4:c.*107G>T MANE Select | NP_777596.2:n.*107G>T | |
| NR_110451.2:n.1793G>T |