Linked Data
ClinVar Variation Id:
482928
dbSNP Id:
rs774452090
gnomAD v2:
17-41219676-T-C
gnomAD v3:
17-43067659-T-C
gnomAD v4:
17-43067659-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43067659T>C , CM000679.2:g.43067659T>C | GRCh38 |
| NC_000017.10:g.41219676T>C , CM000679.1:g.41219676T>C | GRCh37 |
| NC_000017.9:g.38473202T>C | NCBI36 |
| NG_005905.2:g.150325A>G , LRG_292:g.150325A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.5020A>G | ENSP00000417241.2:p.Thr1674Ala | |
| ENST00000470026.6:c.5023A>G | ENSP00000419274.2:p.Thr1675Ala | |
| ENST00000473961.6:c.4897A>G | ENSP00000420201.2:p.Thr1633Ala | |
| ENST00000476777.6:c.5017A>G | ENSP00000417554.2:p.Thr1673Ala | |
| ENST00000477152.6:c.4945A>G | ENSP00000419988.2:p.Thr1649Ala | |
| ENST00000478531.6:c.1711A>G | ENSP00000420412.2:p.Thr571Ala | |
| ENST00000489037.2:c.4945A>G | ENSP00000420781.2:p.Thr1649Ala | |
| ENST00000493919.6:c.1573A>G | ENSP00000418819.2:p.Thr525Ala | |
| ENST00000494123.6:c.5023A>G | ENSP00000419103.2:p.Thr1675Ala | |
| ENST00000497488.2:c.4135A>G | ENSP00000418986.2:p.Thr1379Ala | |
| ENST00000618469.2:c.5023A>G | ENSP00000478114.2:p.Thr1675Ala | |
| ENST00000634433.2:c.4900A>G | ENSP00000489431.2:p.Thr1634Ala | |
| ENST00000644379.2:c.5089A>G | ENSP00000496570.2:p.Thr1697Ala | |
| ENST00000644555.2:c.1573A>G | ENSP00000494614.2:p.Thr525Ala | |
| ENST00000652672.2:c.4882A>G | ENSP00000498906.2:p.Thr1628Ala | |
| ENST00000484087.6:c.1585A>G | ENSP00000419481.2:p.Thr529Ala | |
| ENST00000357654.9:c.5023A>G MANE Select | ENSP00000350283.3:p.Thr1675Ala | |
| ENST00000471181.7:c.5086A>G | ENSP00000418960.2:p.Thr1696Ala | |
| ENST00000644379.1:c.1410A>G | ||
| ENST00000352993.7:c.1597A>G | ENSP00000312236.5:p.Thr533Ala | |
| ENST00000357654.7:c.5023A>G | ENSP00000350283.3:p.Thr1675Ala | |
| ENST00000461221.5:c.*4806A>G | ENSP00000418548.1:n.*4806A>G | |
| ENST00000468300.5:c.1711A>G | ENSP00000417148.1:p.Thr571Ala | |
| ENST00000471181.6:c.5086A>G | ENSP00000418960.2:p.Thr1696Ala | |
| ENST00000472490.1:n.176A>G | ||
| ENST00000478531.5:c.1711A>G | ENSP00000420412.1:p.Thr571Ala | |
| ENST00000484087.5:c.1336A>G | ENSP00000419481.1:p.Thr446Ala | |
| ENST00000491747.6:c.1711A>G | ENSP00000420705.2:p.Thr571Ala | |
| ENST00000493795.5:c.4882A>G | ENSP00000418775.1:p.Thr1628Ala | |
| ENST00000493919.5:c.1573A>G | ENSP00000418819.1:p.Thr525Ala | |
| ENST00000586385.5:c.5-3708A>G | ENSP00000465818.1:n.5-3708A>G | |
| ENST00000591534.5:c.496A>G | ENSP00000467329.1:p.Thr166Ala | |
| ENST00000591849.5:c.-98-17469A>G | ENSP00000465347.1:n.-98-17469A>G | |
| NM_007294.3:c.5023A>G , LRG_292t1:c.5023A>G | NP_009225.1:p.Thr1675Ala | |
| NM_007297.3:c.4882A>G | NP_009228.2:p.Thr1628Ala | |
| NM_007298.3:c.1711A>G | NP_009229.2:p.Thr571Ala | |
| NM_007299.3:c.1711A>G | NP_009230.2:p.Thr571Ala | |
| NM_007300.3:c.5086A>G | NP_009231.2:p.Thr1696Ala | |
| NR_027676.1:n.5159A>G | ||
| NM_007294.4:c.5023A>G MANE Select | NP_009225.1:p.Thr1675Ala | |
| NM_007297.4:c.4882A>G | NP_009228.2:p.Thr1628Ala | |
| NM_007299.4:c.1711A>G | NP_009230.2:p.Thr571Ala | |
| NM_007300.4:c.5086A>G | NP_009231.2:p.Thr1696Ala | |
| NR_027676.2:n.5200A>G |