Linked Data
ClinVar Variation Id:
13858
ClinVar RCV Id:
RCV000014872
dbSNP Id:
rs121913684
COSMIC:
COSM51381
PubMed:
PMID:9450866
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54733094A>G , CM000666.2:g.54733094A>G | GRCh38 |
| NC_000004.11:g.55599260A>G , CM000666.1:g.55599260A>G | GRCh37 |
| NC_000004.10:g.55294017A>G | NCBI36 |
| NG_007456.1:g.80100A>G , LRG_307:g.80100A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412167.7:c.2374A>G | ENSP00000390987.3:p.Arg792Gly | |
| ENST00000685269.1:n.2464A>G | ||
| ENST00000686011.1:c.2371A>G | ENSP00000509704.1:p.Arg791Gly | |
| ENST00000687109.1:c.2389A>G | ENSP00000509371.1:p.Arg797Gly | |
| ENST00000687208.1:n.2798A>G | ||
| ENST00000687246.1:c.2349+1096A>G | ENSP00000509114.1:n.2349+1096A>G | |
| ENST00000687265.1:n.2544A>G | ||
| ENST00000687295.1:c.2374A>G | ENSP00000509450.1:p.Arg792Gly | |
| ENST00000688060.1:n.183A>G | ||
| ENST00000688704.1:n.1398A>G | ||
| ENST00000689832.1:c.2386A>G | ENSP00000509084.1:p.Arg796Gly | |
| ENST00000689994.1:c.1876A>G | ENSP00000509156.1:p.Arg626Gly | |
| ENST00000690543.1:c.2377A>G | ENSP00000508831.1:p.Arg793Gly | |
| ENST00000690917.1:n.2604A>G | ||
| ENST00000691361.1:n.1296A>G | ||
| ENST00000692783.1:c.2383A>G | ENSP00000508733.1:p.Arg795Gly | |
| ENST00000692991.1:n.2483A>G | ||
| ENST00000288135.6:c.2386A>G MANE Select | ENSP00000288135.6:p.Arg796Gly | |
| ENST00000288135.5:c.2386A>G | ENSP00000288135.5:p.Arg796Gly | |
| ENST00000412167.6:c.2374A>G | ENSP00000390987.2:p.Arg792Gly | |
| ENST00000512959.1:n.439A>G | ||
| NM_000222.2:c.2386A>G , LRG_307t1:c.2386A>G | NP_000213.1:p.Arg796Gly | |
| NM_001093772.1:c.2374A>G | NP_001087241.1:p.Arg792Gly | |
| XM_005265740.1:c.2389A>G | XP_005265797.1:p.Arg797Gly | |
| XM_005265741.1:c.2386A>G | XP_005265798.1:p.Arg796Gly | |
| XM_005265742.1:c.2377A>G | XP_005265799.1:p.Arg793Gly | |
| XM_005265742.3:c.2377A>G | XP_005265799.1:p.Arg793Gly | |
| XM_017008178.1:c.2383A>G | XP_016863667.1:p.Arg795Gly | |
| XM_017008179.1:c.2374A>G | XP_016863668.1:p.Arg792Gly | |
| XM_017008180.1:c.2371A>G | XP_016863669.1:p.Arg791Gly | |
| NM_000222.3:c.2386A>G MANE Select | NP_000213.1:p.Arg796Gly | |
| NM_001093772.2:c.2374A>G | NP_001087241.1:p.Arg792Gly | |
| NM_001385284.1:c.2389A>G | NP_001372213.1:p.Arg797Gly | |
| NM_001385285.1:c.2383A>G | NP_001372214.1:p.Arg795Gly | |
| NM_001385286.1:c.2371A>G | NP_001372215.1:p.Arg791Gly | |
| NM_001385288.1:c.2377A>G | NP_001372217.1:p.Arg793Gly | |
| NM_001385290.1:c.2386A>G | NP_001372219.1:p.Arg796Gly | |
| NM_001385292.1:c.2374A>G | NP_001372221.1:p.Arg792Gly |