Linked Data
dbSNP Id:
rs1463483725
gnomAD v2:
18-29101069-G-T
gnomAD v4:
18-31521106-G-T
COSMIC:
COSM5651175
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31521106G>T , CM000680.2:g.31521106G>T | GRCh38 |
| NC_000018.9:g.29101069G>T , CM000680.1:g.29101069G>T | GRCh37 |
| NC_000018.8:g.27355067G>T | NCBI36 |
| NG_007072.3:g.27865G>T , LRG_397:g.27865G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682087.2:n.217G>T | ||
| ENST00000682241.2:c.386G>T | ENSP00000507600.2:p.Gly129Val | |
| ENST00000683614.2:n.217G>T | ||
| ENST00000682087.1:c.217G>T | ||
| ENST00000682241.1:c.217G>T | ||
| ENST00000683614.1:c.217G>T | ||
| ENST00000683654.1:c.386G>T | ENSP00000506971.1:p.Gly129Val | |
| ENST00000684461.1:n.217G>T | ||
| ENST00000261590.13:c.386G>T MANE Select | ENSP00000261590.8:p.Gly129Val | |
| ENST00000261590.12:c.386G>T | ENSP00000261590.8:p.Gly129Val | |
| ENST00000585206.1:c.386G>T | ENSP00000462503.1:p.Gly129Val | |
| NM_001943.3:c.386G>T , LRG_397t1:c.386G>T | NP_001934.2:p.Gly129Val | |
| NM_001943.4:c.386G>T | NP_001934.2:p.Gly129Val | |
| XM_024451095.1:c.-149G>T | XP_024306863.1:n.-149G>T | |
| NM_001943.5:c.386G>T MANE Select | NP_001934.2:p.Gly129Val |