dbSNP:
Revel Score:
ENST00000218099 (MANE Select)
0.988
ENST00000394090
0.988
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561911G>T , CM000685.2:g.139561911G>T | GRCh38 |
| NC_000023.10:g.138644070G>T , CM000685.1:g.138644070G>T | GRCh37 |
| NC_000023.9:g.138471736G>T | NCBI36 |
| NG_007994.1:g.36176G>T , LRG_556:g.36176G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.1226G>T MANE Select | ENSP00000218099.2:p.Gly409Val | |
| ENST00000643157.1:n.1723+170G>T | ||
| ENST00000218099.6:c.1226G>T | ENSP00000218099.2:p.Gly409Val | |
| ENST00000394090.2:c.1112G>T | ENSP00000377650.2:p.Gly371Val | |
| NM_000133.3:c.1226G>T , LRG_556t1:c.1226G>T | NP_000124.1:p.Gly409Val | |
| NM_001313913.1:c.1112G>T | NP_001300842.1:p.Gly371Val | |
| XM_005262397.3:c.1097G>T | XP_005262454.1:p.Gly366Val | |
| XM_005262397.4:c.1097G>T | XP_005262454.1:p.Gly366Val | |
| NM_000133.4:c.1226G>T MANE Select | NP_000124.1:p.Gly409Val | |
| NM_001313913.2:c.1112G>T | NP_001300842.1:p.Gly371Val |