Linked Data
ClinVar Variation Id:
441375
dbSNP Id:
rs778487856
ExAC:
17:41222982 A / G
gnomAD v2:
17-41222982-A-G
gnomAD v3:
17-43070965-A-G
gnomAD v4:
17-43070965-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43070965A>G , CM000679.2:g.43070965A>G | GRCh38 |
| NC_000017.10:g.41222982A>G , CM000679.1:g.41222982A>G | GRCh37 |
| NC_000017.9:g.38476508A>G | NCBI36 |
| NG_005905.2:g.147019T>C , LRG_292:g.147019T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4946T>C | ENSP00000417241.2:p.Met1649Thr | |
| ENST00000470026.6:c.4949T>C | ENSP00000419274.2:p.Met1650Thr | |
| ENST00000473961.6:c.4823T>C | ENSP00000420201.2:p.Met1608Thr | |
| ENST00000476777.6:c.4943T>C | ENSP00000417554.2:p.Met1648Thr | |
| ENST00000477152.6:c.4871T>C | ENSP00000419988.2:p.Met1624Thr | |
| ENST00000478531.6:c.1637T>C | ENSP00000420412.2:p.Met546Thr | |
| ENST00000489037.2:c.4871T>C | ENSP00000420781.2:p.Met1624Thr | |
| ENST00000493919.6:c.1499T>C | ENSP00000418819.2:p.Met500Thr | |
| ENST00000494123.6:c.4949T>C | ENSP00000419103.2:p.Met1650Thr | |
| ENST00000497488.2:c.4061T>C | ENSP00000418986.2:p.Met1354Thr | |
| ENST00000618469.2:c.4949T>C | ENSP00000478114.2:p.Met1650Thr | |
| ENST00000634433.2:c.4826T>C | ENSP00000489431.2:p.Met1609Thr | |
| ENST00000644379.2:c.5015T>C | ENSP00000496570.2:p.Met1672Thr | |
| ENST00000644555.2:c.1499T>C | ENSP00000494614.2:p.Met500Thr | |
| ENST00000652672.2:c.4808T>C | ENSP00000498906.2:p.Met1603Thr | |
| ENST00000484087.6:c.1511T>C | ENSP00000419481.2:p.Met504Thr | |
| ENST00000700182.1:c.1556T>C | ENSP00000514849.1:p.Met519Thr | |
| ENST00000357654.9:c.4949T>C MANE Select | ENSP00000350283.3:p.Met1650Thr | |
| ENST00000471181.7:c.5012T>C | ENSP00000418960.2:p.Met1671Thr | |
| ENST00000644379.1:c.1336T>C | ||
| ENST00000352993.7:c.1523T>C | ENSP00000312236.5:p.Met508Thr | |
| ENST00000357654.7:c.4949T>C | ENSP00000350283.3:p.Met1650Thr | |
| ENST00000461221.5:c.*4732T>C | ENSP00000418548.1:n.*4732T>C | |
| ENST00000468300.5:c.1637T>C | ENSP00000417148.1:p.Met546Thr | |
| ENST00000471181.6:c.5012T>C | ENSP00000418960.2:p.Met1671Thr | |
| ENST00000472490.1:n.102T>C | ||
| ENST00000478531.5:c.1637T>C | ENSP00000420412.1:p.Met546Thr | |
| ENST00000484087.5:c.1262T>C | ENSP00000419481.1:p.Met421Thr | |
| ENST00000491747.6:c.1637T>C | ENSP00000420705.2:p.Met546Thr | |
| ENST00000493795.5:c.4808T>C | ENSP00000418775.1:p.Met1603Thr | |
| ENST00000493919.5:c.1499T>C | ENSP00000418819.1:p.Met500Thr | |
| ENST00000586385.5:c.5-7014T>C | ENSP00000465818.1:n.5-7014T>C | |
| ENST00000591534.5:c.422T>C | ENSP00000467329.1:p.Met141Thr | |
| ENST00000591849.5:c.-98-20775T>C | ENSP00000465347.1:n.-98-20775T>C | |
| NM_007294.3:c.4949T>C , LRG_292t1:c.4949T>C | NP_009225.1:p.Met1650Thr | |
| NM_007297.3:c.4808T>C | NP_009228.2:p.Met1603Thr | |
| NM_007298.3:c.1637T>C | NP_009229.2:p.Met546Thr | |
| NM_007299.3:c.1637T>C | NP_009230.2:p.Met546Thr | |
| NM_007300.3:c.5012T>C | NP_009231.2:p.Met1671Thr | |
| NR_027676.1:n.5085T>C | ||
| NM_007294.4:c.4949T>C MANE Select | NP_009225.1:p.Met1650Thr | |
| NM_007297.4:c.4808T>C | NP_009228.2:p.Met1603Thr | |
| NM_007299.4:c.1637T>C | NP_009230.2:p.Met546Thr | |
| NM_007300.4:c.5012T>C | NP_009231.2:p.Met1671Thr | |
| NR_027676.2:n.5126T>C |