Linked Data
ClinVar Variation Id:
1435072
ClinVar RCV Id:
RCV001955243
dbSNP Id:
rs142760483
gnomAD v4:
9-135770436-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135770436C>A , CM000671.2:g.135770436C>A | GRCh38 |
| NC_000009.11:g.138662282C>A , CM000671.1:g.138662282C>A | GRCh37 |
| NC_000009.10:g.137802103C>A | NCBI36 |
| NG_033070.1:g.73252C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.1758C>A MANE Select | ENSP00000360822.2:p.His586Gln | |
| ENST00000674572.1:c.1599C>A | ENSP00000501742.1:p.His533Gln | |
| ENST00000675090.1:c.1506C>A | ENSP00000501833.1:p.His502Gln | |
| ENST00000675399.1:c.1506C>A | ENSP00000501932.1:p.His502Gln | |
| ENST00000676421.1:c.1515C>A | ENSP00000502322.1:p.His505Gln | |
| ENST00000263604.5:c.1659C>A | ENSP00000263604.4:p.His553Gln | |
| ENST00000371757.6:c.1758C>A | ENSP00000360822.2:p.His586Gln | |
| ENST00000460750.5:c.*1368C>A | ENSP00000418777.1:n.*1368C>A | |
| ENST00000486577.6:c.1641C>A | ENSP00000417578.3:p.His547Gln | |
| ENST00000487664.5:c.1758C>A | ENSP00000417851.2:p.His586Gln | |
| ENST00000488444.6:c.1701C>A | ENSP00000419007.3:p.His567Gln | |
| ENST00000490355.6:c.1701C>A | ENSP00000418003.3:p.His567Gln | |
| ENST00000490363.3:n.1577C>A | ||
| ENST00000491806.6:c.1701C>A | ENSP00000419086.3:p.His567Gln | |
| ENST00000628528.2:c.1623C>A | ENSP00000486374.1:p.His541Gln | |
| ENST00000630792.2:c.1599C>A | ENSP00000486486.1:p.His533Gln | |
| ENST00000631073.2:c.1701C>A | ENSP00000486130.1:p.His567Gln | |
| NM_001272003.1:c.1623C>A | NP_001258932.1:p.His541Gln | |
| NM_020822.2:c.1758C>A | NP_065873.2:p.His586Gln | |
| XM_011518877.1:c.1893C>A | XP_011517179.1:p.His631Gln | |
| XM_011518878.1:c.1902C>A | XP_011517180.1:p.His634Gln | |
| XM_011518879.1:c.1893C>A | XP_011517181.1:p.His631Gln | |
| XM_011518880.1:c.1659C>A | XP_011517182.1:p.His553Gln | |
| XM_011518881.1:c.1248C>A | XP_011517183.1:p.His416Gln | |
| XM_011518877.3:c.1893C>A | XP_011517179.1:p.His631Gln | |
| XM_011518878.3:c.1902C>A | XP_011517180.1:p.His634Gln | |
| XM_011518879.3:c.1893C>A | XP_011517181.1:p.His631Gln | |
| XM_011518881.3:c.1248C>A | XP_011517183.1:p.His416Gln | |
| XM_017014931.1:c.1692C>A | XP_016870420.1:p.His564Gln | |
| XM_017014932.1:c.1515C>A | XP_016870421.1:p.His505Gln | |
| XM_017014933.1:c.1248C>A | XP_016870422.1:p.His416Gln | |
| XM_024447617.1:c.1248C>A | XP_024303385.1:p.His416Gln | |
| XM_024447618.1:c.1248C>A | XP_024303386.1:p.His416Gln | |
| NM_020822.3:c.1758C>A MANE Select | NP_065873.2:p.His586Gln | |
| NM_001272003.2:c.1623C>A | NP_001258932.1:p.His541Gln |