Linked Data
ClinVar Variation Id:
456439
ClinVar RCV Id:
RCV000551801
dbSNP Id:
rs757356178
ExAC:
17:78081446 C / T
gnomAD v2:
17-78081446-C-T
gnomAD v3:
17-80107647-C-T
gnomAD v4:
17-80107647-C-T
COSMIC:
COSM985504
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80107647C>T , CM000679.2:g.80107647C>T | GRCh38 |
| NC_000017.10:g.78081446C>T , CM000679.1:g.78081446C>T | GRCh37 |
| NC_000017.9:g.75696041C>T | NCBI36 |
| NG_009822.1:g.11092C>T , LRG_673:g.11092C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570803.6:c.783C>T | ENSP00000460543.2:p.Ala261= | |
| ENST00000572080.2:c.783C>T | ENSP00000459972.2:p.Ala261= | |
| ENST00000577106.6:c.783C>T | ENSP00000458306.2:p.Ala261= | |
| ENST00000302262.8:c.783C>T MANE Select | ENSP00000305692.3:p.Ala261= | |
| ENST00000302262.7:c.783C>T | ENSP00000305692.3:p.Ala261= | |
| ENST00000390015.7:c.783C>T | ENSP00000374665.3:p.Ala261= | |
| ENST00000570803.5:c.783C>T | ENSP00000460543.1:p.Ala261= | |
| NM_000152.3:c.783C>T , LRG_673t1:c.783C>T | NP_000143.2:p.Ala261= | |
| NM_001079803.1:c.783C>T | NP_001073271.1:p.Ala261= | |
| NM_001079804.1:c.783C>T | NP_001073272.1:p.Ala261= | |
| XM_005257193.1:c.783C>T | XP_005257250.1:p.Ala261= | |
| XM_005257194.3:c.783C>T | XP_005257251.1:p.Ala261= | |
| NM_000152.4:c.783C>T | NP_000143.2:p.Ala261= | |
| NM_001079803.2:c.783C>T | NP_001073271.1:p.Ala261= | |
| NM_001079804.2:c.783C>T | NP_001073272.1:p.Ala261= | |
| XM_005257193.2:c.783C>T | XP_005257250.1:p.Ala261= | |
| XM_005257194.4:c.783C>T | XP_005257251.1:p.Ala261= | |
| NM_000152.5:c.783C>T MANE Select | NP_000143.2:p.Ala261= | |
| NM_001079803.3:c.783C>T | NP_001073271.1:p.Ala261= | |
| NM_001079804.3:c.783C>T | NP_001073272.1:p.Ala261= |