Revel Score:
ENST00000496887
0.739
ENST00000155840 (MANE Select)
0.739
ENST00000335475
0.739
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00049473 (AFR)
Genomes Max Group AF
0.00049807 (AFR)
Exomes Max Group AF
0.0003711 (AFR)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2527999C>T , CM000673.2:g.2527999C>T | GRCh38 |
| NC_000011.9:g.2549229C>T , CM000673.1:g.2549229C>T | GRCh37 |
| NC_000011.8:g.2505805C>T | NCBI36 |
| NG_008935.1:g.88009C>T , LRG_287:g.88009C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.197C>T | ENSP00000434560.2:p.Thr66Met | |
| ENST00000646564.2:c.458C>T | ENSP00000495806.2:p.Thr153Met | |
| ENST00000155840.12:c.458C>T MANE Select | ENSP00000155840.2:p.Thr153Met | |
| ENST00000335475.6:c.77C>T | ENSP00000334497.5:p.Thr26Met | |
| ENST00000646564.1:c.104C>T | ENSP00000495806.1:p.Thr35Met | |
| ENST00000155840.9:c.458C>T | ENSP00000155840.2:p.Thr153Met | |
| ENST00000335475.5:c.77C>T | ENSP00000334497.5:p.Thr26Met | |
| ENST00000496887.6:c.197C>T | ENSP00000434560.1:p.Thr66Met | |
| NM_000218.2:c.458C>T , LRG_287t1:c.458C>T | NP_000209.2:p.Thr153Met | |
| NM_181798.1:c.77C>T , LRG_287t2:c.77C>T | NP_861463.1:p.Thr26Met | |
| NM_000218.3:c.458C>T MANE Select | NP_000209.2:p.Thr153Met |