Linked Data
ClinVar Variation Id:
282311
dbSNP Id:
rs770248553
ExAC:
17:78086733 C / T
gnomAD v2:
17-78086733-C-T
gnomAD v4:
17-80112934-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80112934C>T , CM000679.2:g.80112934C>T | GRCh38 |
| NC_000017.10:g.78086733C>T , CM000679.1:g.78086733C>T | GRCh37 |
| NC_000017.9:g.75701328C>T | NCBI36 |
| NG_009822.1:g.16379C>T , LRG_673:g.16379C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570803.6:c.1947C>T | ENSP00000460543.2:p.Phe649= | |
| ENST00000572080.2:c.*85C>T | ENSP00000459972.2:n.*85C>T | |
| ENST00000577106.6:c.1947C>T | ENSP00000458306.2:p.Phe649= | |
| ENST00000302262.8:c.1947C>T MANE Select | ENSP00000305692.3:p.Phe649= | |
| ENST00000302262.7:c.1947C>T | ENSP00000305692.3:p.Phe649= | |
| ENST00000390015.7:c.1947C>T | ENSP00000374665.3:p.Phe649= | |
| ENST00000570716.1:n.387C>T | ||
| ENST00000572080.1:c.366C>T | ||
| ENST00000572803.1:n.561C>T | ||
| NM_000152.3:c.1947C>T , LRG_673t1:c.1947C>T | NP_000143.2:p.Phe649= | |
| NM_001079803.1:c.1947C>T | NP_001073271.1:p.Phe649= | |
| NM_001079804.1:c.1947C>T | NP_001073272.1:p.Phe649= | |
| XM_005257193.1:c.1947C>T | XP_005257250.1:p.Phe649= | |
| XM_005257194.3:c.1947C>T | XP_005257251.1:p.Phe649= | |
| NM_000152.4:c.1947C>T | NP_000143.2:p.Phe649= | |
| NM_001079803.2:c.1947C>T | NP_001073271.1:p.Phe649= | |
| NM_001079804.2:c.1947C>T | NP_001073272.1:p.Phe649= | |
| XM_005257193.2:c.1947C>T | XP_005257250.1:p.Phe649= | |
| XM_005257194.4:c.1947C>T | XP_005257251.1:p.Phe649= | |
| NM_000152.5:c.1947C>T MANE Select | NP_000143.2:p.Phe649= | |
| NM_001079803.3:c.1947C>T | NP_001073271.1:p.Phe649= | |
| NM_001079804.3:c.1947C>T | NP_001073272.1:p.Phe649= |