Linked Data
ClinVar Variation Id:
2027135
ClinVar RCV Id:
RCV002871710
dbSNP Id:
rs1567789643
MyVariant Identifiers:
chr17:g.41243642T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43091625T>C , CM000679.2:g.43091625T>C | GRCh38 |
| NC_000017.10:g.41243642T>C , CM000679.1:g.41243642T>C | GRCh37 |
| NC_000017.9:g.38497168T>C | NCBI36 |
| NG_005905.2:g.126359A>G , LRG_292:g.126359A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3970A>G | ||
| ENST00000461574.2:c.3906A>G | ENSP00000417241.2:p.Glu1302= | |
| ENST00000470026.6:c.3906A>G | ENSP00000419274.2:p.Glu1302= | |
| ENST00000473961.6:c.3780A>G | ENSP00000420201.2:p.Glu1260= | |
| ENST00000476777.6:c.3903A>G | ENSP00000417554.2:p.Glu1301= | |
| ENST00000477152.6:c.3828A>G | ENSP00000419988.2:p.Glu1276= | |
| ENST00000478531.6:c.785-593A>G | ENSP00000420412.2:n.785-593A>G | |
| ENST00000489037.2:c.3828A>G | ENSP00000420781.2:p.Glu1276= | |
| ENST00000493919.6:c.647-593A>G | ENSP00000418819.2:n.647-593A>G | |
| ENST00000494123.6:c.3906A>G | ENSP00000419103.2:p.Glu1302= | |
| ENST00000497488.2:c.3018A>G | ENSP00000418986.2:p.Glu1006= | |
| ENST00000618469.2:c.3906A>G | ENSP00000478114.2:p.Glu1302= | |
| ENST00000634433.2:c.3783A>G | ENSP00000489431.2:p.Glu1261= | |
| ENST00000644379.2:c.3906A>G | ENSP00000496570.2:p.Glu1302= | |
| ENST00000644555.2:c.647-593A>G | ENSP00000494614.2:n.647-593A>G | |
| ENST00000652672.2:c.3765A>G | ENSP00000498906.2:p.Glu1255= | |
| ENST00000484087.6:c.665-593A>G | ENSP00000419481.2:n.665-593A>G | |
| ENST00000700182.1:c.707-593A>G | ENSP00000514849.1:n.707-593A>G | |
| ENST00000357654.9:c.3906A>G MANE Select | ENSP00000350283.3:p.Glu1302= | |
| ENST00000471181.7:c.3906A>G | ENSP00000418960.2:p.Glu1302= | |
| ENST00000644379.1:c.227A>G | ||
| ENST00000352993.7:c.671-593A>G | ENSP00000312236.5:n.671-593A>G | |
| ENST00000354071.7:c.3906A>G | ENSP00000326002.7:p.Glu1302= | |
| ENST00000357654.7:c.3906A>G | ENSP00000350283.3:p.Glu1302= | |
| ENST00000461221.5:c.*3689A>G | ENSP00000418548.1:n.*3689A>G | |
| ENST00000461574.1:c.200A>G | ||
| ENST00000468300.5:c.788-593A>G | ENSP00000417148.1:n.788-593A>G | |
| ENST00000471181.6:c.3906A>G | ENSP00000418960.2:p.Glu1302= | |
| ENST00000478531.5:c.785-593A>G | ENSP00000420412.1:n.785-593A>G | |
| ENST00000484087.5:c.410-593A>G | ENSP00000419481.1:n.410-593A>G | |
| ENST00000487825.5:c.413-593A>G | ENSP00000418212.1:n.413-593A>G | |
| ENST00000491747.6:c.788-593A>G | ENSP00000420705.2:n.788-593A>G | |
| ENST00000493795.5:c.3765A>G | ENSP00000418775.1:p.Glu1255= | |
| ENST00000493919.5:c.647-593A>G | ENSP00000418819.1:n.647-593A>G | |
| ENST00000586385.5:c.5-27674A>G | ENSP00000465818.1:n.5-27674A>G | |
| ENST00000591534.5:c.-43-17104A>G | ENSP00000467329.1:n.-43-17104A>G | |
| ENST00000591849.5:c.-99+33646A>G | ENSP00000465347.1:n.-99+33646A>G | |
| NM_007294.3:c.3906A>G , LRG_292t1:c.3906A>G | NP_009225.1:p.Glu1302= | |
| NM_007297.3:c.3765A>G | NP_009228.2:p.Glu1255= | |
| NM_007298.3:c.788-593A>G | NP_009229.2:n.788-593A>G | |
| NM_007299.3:c.788-593A>G | NP_009230.2:n.788-593A>G | |
| NM_007300.3:c.3906A>G | NP_009231.2:p.Glu1302= | |
| NR_027676.1:n.4042A>G | ||
| NM_007294.4:c.3906A>G MANE Select | NP_009225.1:p.Glu1302= | |
| NM_007297.4:c.3765A>G | NP_009228.2:p.Glu1255= | |
| NM_007299.4:c.788-593A>G | NP_009230.2:n.788-593A>G | |
| NM_007300.4:c.3906A>G | NP_009231.2:p.Glu1302= | |
| NR_027676.2:n.4083A>G |