Linked Data
ClinVar Variation Id:
410360
dbSNP Id:
rs895543540
gnomAD v2:
3-121981165-C-T
gnomAD v3:
3-122262318-C-T
gnomAD v4:
3-122262318-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122262318C>T , CM000665.2:g.122262318C>T | GRCh38 |
| NC_000003.11:g.121981165C>T , CM000665.1:g.121981165C>T | GRCh37 |
| NC_000003.10:g.123463855C>T | NCBI36 |
| NG_009058.1:g.83636C>T | |
| NG_009058.2:g.83651C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490131.7:c.1283C>T | ENSP00000418685.2:p.Ala428Val | |
| ENST00000498619.4:c.1283C>T | ENSP00000420194.1:p.Ala428Val | |
| ENST00000638421.1:c.1283C>T | ENSP00000492190.1:p.Ala428Val | |
| ENST00000639785.2:c.1283C>T MANE Select | ENSP00000491584.2:p.Ala428Val | |
| ENST00000490131.5:c.1283C>T | ENSP00000418685.1:p.Ala428Val | |
| ENST00000498619.2:c.1283C>T | ENSP00000420194.1:p.Ala428Val | |
| NM_000388.3:c.1283C>T | NP_000379.2:p.Ala428Val | |
| NM_001178065.1:c.1283C>T | NP_001171536.1:p.Ala428Val | |
| XM_005247836.2:c.1283C>T | XP_005247893.1:p.Ala428Val | |
| XM_005247837.2:c.800C>T | XP_005247894.1:p.Ala267Val | |
| XM_006713789.2:c.1283C>T | XP_006713852.1:p.Ala428Val | |
| XM_011513237.1:c.1283C>T | XP_011511539.1:p.Ala428Val | |
| XM_011513238.1:c.1283C>T | XP_011511540.1:p.Ala428Val | |
| XM_011513239.1:c.695C>T | XP_011511541.1:p.Ala232Val | |
| XM_006713789.3:c.1283C>T | XP_006713852.1:p.Ala428Val | |
| XM_017007324.1:c.1283C>T | XP_016862813.1:p.Ala428Val | |
| XM_017007325.1:c.1283C>T | XP_016862814.1:p.Ala428Val | |
| NM_000388.4:c.1283C>T MANE Select | NP_000379.3:p.Ala428Val | |
| NM_001178065.2:c.1283C>T | NP_001171536.2:p.Ala428Val |