Linked Data
ClinVar Variation Id:
2944156
ClinVar RCV Id:
RCV003805906
dbSNP Id:
rs2126590349
MyVariant Identifiers:
chr5:g.236668C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.236553C>G , CM000667.2:g.236553C>G | GRCh38 |
| NC_000005.9:g.236668C>G , CM000667.1:g.236668C>G | GRCh37 |
| NC_000005.8:g.289668C>G | NCBI36 |
| NG_012339.1:g.23313C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264932.11:c.1386C>G MANE Select | ENSP00000264932.6:p.Val462= | |
| ENST00000651543.1:c.*119C>G | ENSP00000499215.1:n.*119C>G | |
| ENST00000264932.10:c.1386C>G | ENSP00000264932.6:p.Val462= | |
| ENST00000504309.5:c.1386C>G | ENSP00000426514.1:p.Val462= | |
| ENST00000505555.5:n.1426C>G | ||
| ENST00000510361.5:c.1242C>G | ENSP00000427703.1:p.Val414= | |
| ENST00000511810.5:n.2133C>G | ||
| ENST00000514027.5:n.1341C>G | ||
| ENST00000515752.5:n.972C>G | ||
| ENST00000515815.5:c.41C>G | ||
| ENST00000617470.4:c.951C>G | ENSP00000484230.1:p.Val317= | |
| NM_001294332.1:c.1242C>G | NP_001281261.1:p.Val414= | |
| NM_004168.3:c.1386C>G | NP_004159.2:p.Val462= | |
| XM_005248331.2:c.1386C>G | XP_005248388.1:p.Val462= | |
| XM_011514072.1:c.1386C>G | XP_011512374.1:p.Val462= | |
| XM_011514073.1:c.1386C>G | XP_011512375.1:p.Val462= | |
| XR_925638.1:n.1519C>G | ||
| NM_001330758.1:c.1386C>G | NP_001317687.1:p.Val462= | |
| XM_011514072.2:c.1386C>G | XP_011512374.1:p.Val462= | |
| XM_011514073.2:c.1386C>G | XP_011512375.1:p.Val462= | |
| XM_017009685.2:c.1386C>G | XP_016865174.1:p.Val462= | |
| XM_024446143.1:c.1242C>G | XP_024301911.1:p.Val414= | |
| XR_002956167.1:n.1433C>G | ||
| NM_004168.4:c.1386C>G MANE Select | NP_004159.2:p.Val462= | |
| NM_001294332.2:c.1242C>G | NP_001281261.1:p.Val414= | |
| NM_001330758.2:c.1386C>G | NP_001317687.1:p.Val462= |