Linked Data
ClinVar Variation Id:
2149090
ClinVar RCV Id:
RCV003081316
MyVariant Identifiers:
chr10:g.79797056C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.78037298C>G , CM000672.2:g.78037298C>G | GRCh38 |
| NC_000010.10:g.79797056C>G , CM000672.1:g.79797056C>G | GRCh37 |
| NC_000010.9:g.79467062C>G | NCBI36 |
| NG_012633.1:g.8539C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360830.9:c.384C>G | ENSP00000354074.5:p.Gly128= | |
| ENST00000372360.9:c.384C>G MANE Select | ENSP00000361435.4:p.Gly128= | |
| ENST00000440692.6:c.384C>G | ENSP00000414321.1:p.Gly128= | |
| ENST00000464716.6:c.384C>G | ENSP00000494231.1:p.Gly128= | |
| ENST00000465692.2:n.395C>G | ||
| ENST00000476545.6:c.384C>G | ENSP00000494169.1:p.Gly128= | |
| ENST00000478655.6:n.423C>G | ||
| ENST00000485708.7:n.423C>G | ||
| ENST00000613865.5:c.384C>G | ENSP00000478869.2:p.Gly128= | |
| ENST00000645195.1:c.260C>G | ||
| ENST00000645440.1:c.384C>G | ENSP00000496738.1:p.Gly128= | |
| ENST00000645698.1:n.412C>G | ||
| ENST00000360830.8:c.384C>G | ENSP00000354074.4:p.Gly128= | |
| ENST00000372360.7:c.384C>G | ENSP00000361435.3:p.Gly128= | |
| ENST00000435275.5:c.384C>G | ENSP00000415549.1:p.Gly128= | |
| ENST00000440692.5:c.384C>G | ENSP00000414321.1:p.Gly128= | |
| ENST00000464716.5:n.412C>G | ||
| ENST00000465692.1:n.381C>G | ||
| ENST00000476545.5:n.408C>G | ||
| ENST00000478655.5:n.423C>G | ||
| ENST00000482069.5:n.451C>G | ||
| ENST00000485708.6:n.442C>G | ||
| ENST00000613865.4:c.384C>G | ENSP00000478869.1:p.Gly128= | |
| NM_001026.4:c.384C>G | NP_001017.1:p.Gly128= | |
| NM_001142282.1:c.384C>G | NP_001135754.1:p.Gly128= | |
| NM_001142283.1:c.384C>G | NP_001135755.1:p.Gly128= | |
| NM_001142284.1:c.384C>G | NP_001135756.1:p.Gly128= | |
| NM_001142285.1:c.384C>G | NP_001135757.1:p.Gly128= | |
| NM_033022.3:c.384C>G | NP_148982.1:p.Gly128= | |
| XM_011540034.1:c.537C>G | XP_011538336.1:p.Gly179= | |
| XM_011540035.1:c.537C>G | XP_011538337.1:p.Gly179= | |
| XM_011540036.1:c.537C>G | XP_011538338.1:p.Gly179= | |
| XM_011540037.1:c.537C>G | XP_011538339.1:p.Gly179= | |
| XM_011540038.1:c.537C>G | XP_011538340.1:p.Gly179= | |
| NM_001142285.2:c.384C>G | NP_001135757.1:p.Gly128= | |
| NM_033022.4:c.384C>G MANE Select | NP_148982.1:p.Gly128= | |
| NM_001026.5:c.384C>G | NP_001017.1:p.Gly128= | |
| NM_001142282.2:c.384C>G | NP_001135754.1:p.Gly128= | |
| NM_001142283.2:c.384C>G | NP_001135755.1:p.Gly128= | |
| NM_001142284.2:c.384C>G | NP_001135756.1:p.Gly128= |