Linked Data
ClinVar Variation Id:
358685
dbSNP Id:
rs763726060
ExAC:
7:116371841 A / G
gnomAD v2:
7-116371841-A-G
gnomAD v3:
7-116731787-A-G
gnomAD v4:
7-116731787-A-G
COSMIC:
COSM5617386
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.116731787A>G , CM000669.2:g.116731787A>G | GRCh38 |
| NC_000007.13:g.116371841A>G , CM000669.1:g.116371841A>G | GRCh37 |
| NC_000007.12:g.116159077A>G | NCBI36 |
| NG_008996.1:g.64383A>G , LRG_662:g.64383A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000422097.2:c.1320A>G | ENSP00000398776.2:p.Thr440= | |
| ENST00000436117.3:c.1320A>G | ENSP00000410980.2:p.Thr440= | |
| ENST00000318493.11:c.1320A>G | ENSP00000317272.6:p.Thr440= | |
| ENST00000397752.8:c.1320A>G MANE Select | ENSP00000380860.3:p.Thr440= | |
| ENST00000318493.10:c.1320A>G | ENSP00000317272.6:p.Thr440= | |
| ENST00000397752.7:c.1320A>G | ENSP00000380860.3:p.Thr440= | |
| ENST00000436117.2:c.1320A>G | ENSP00000410980.2:p.Thr440= | |
| ENST00000495962.1:n.300A>G | ||
| NM_000245.2:c.1320A>G | NP_000236.2:p.Thr440= | |
| NM_001127500.1:c.1320A>G , LRG_662t1:c.1320A>G | NP_001120972.1:p.Thr440= | |
| XM_006715990.2:c.30A>G | XP_006716053.1:p.Thr10= | |
| XM_006715991.2:c.30A>G | XP_006716054.1:p.Thr10= | |
| XM_011516223.1:c.1377A>G | XP_011514525.1:p.Thr459= | |
| NM_000245.3:c.1320A>G | NP_000236.2:p.Thr440= | |
| NM_001127500.2:c.1320A>G | NP_001120972.1:p.Thr440= | |
| NM_001324401.1:c.1320A>G | NP_001311330.1:p.Thr440= | |
| NM_001324402.1:c.30A>G | NP_001311331.1:p.Thr10= | |
| XR_001744772.1:n.1551A>G | ||
| NM_001127500.3:c.1320A>G | NP_001120972.1:p.Thr440= | |
| NM_000245.4:c.1320A>G MANE Select | NP_000236.2:p.Thr440= | |
| NM_001324401.2:c.1320A>G | NP_001311330.1:p.Thr440= | |
| NM_001324402.2:c.30A>G | NP_001311331.1:p.Thr10= | |
| NM_001324401.3:c.1320A>G | NP_001311330.1:p.Thr440= |