Linked Data
ClinVar Variation Id:
2017803
ClinVar RCV Id:
RCV002857039
MyVariant Identifiers:
chr17:g.78090824C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80117025C>A , CM000679.2:g.80117025C>A | GRCh38 |
| NC_000017.10:g.78090824C>A , CM000679.1:g.78090824C>A | GRCh37 |
| NC_000017.9:g.75705419C>A | NCBI36 |
| NG_009822.1:g.20470C>A , LRG_673:g.20470C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570803.6:c.2247C>A | ENSP00000460543.2:p.Ala749= | |
| ENST00000572080.2:c.*385C>A | ENSP00000459972.2:n.*385C>A | |
| ENST00000577106.6:c.2247C>A | ENSP00000458306.2:p.Ala749= | |
| ENST00000302262.8:c.2247C>A MANE Select | ENSP00000305692.3:p.Ala749= | |
| ENST00000302262.7:c.2247C>A | ENSP00000305692.3:p.Ala749= | |
| ENST00000390015.7:c.2247C>A | ENSP00000374665.3:p.Ala749= | |
| ENST00000572080.1:c.666C>A | ||
| ENST00000573556.1:n.200C>A | ||
| NM_000152.3:c.2247C>A , LRG_673t1:c.2247C>A | NP_000143.2:p.Ala749= | |
| NM_001079803.1:c.2247C>A | NP_001073271.1:p.Ala749= | |
| NM_001079804.1:c.2247C>A | NP_001073272.1:p.Ala749= | |
| XM_005257193.1:c.2247C>A | XP_005257250.1:p.Ala749= | |
| XM_005257194.3:c.2247C>A | XP_005257251.1:p.Ala749= | |
| NM_000152.4:c.2247C>A | NP_000143.2:p.Ala749= | |
| NM_001079803.2:c.2247C>A | NP_001073271.1:p.Ala749= | |
| NM_001079804.2:c.2247C>A | NP_001073272.1:p.Ala749= | |
| XM_005257193.2:c.2247C>A | XP_005257250.1:p.Ala749= | |
| XM_005257194.4:c.2247C>A | XP_005257251.1:p.Ala749= | |
| NM_000152.5:c.2247C>A MANE Select | NP_000143.2:p.Ala749= | |
| NM_001079803.3:c.2247C>A | NP_001073271.1:p.Ala749= | |
| NM_001079804.3:c.2247C>A | NP_001073272.1:p.Ala749= |