Linked Data
ClinVar Variation Id:
37690
dbSNP Id:
rs80357088
ExAC:
17:41247872 C / A
gnomAD v2:
17-41247872-C-A
gnomAD v3:
17-43095855-C-A
gnomAD v4:
17-43095855-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43095855C>A , CM000679.2:g.43095855C>A | GRCh38 |
| NC_000017.10:g.41247872C>A , CM000679.1:g.41247872C>A | GRCh37 |
| NC_000017.9:g.38501398C>A | NCBI36 |
| NG_005905.2:g.122129G>T , LRG_292:g.122129G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.725G>T | ||
| ENST00000461574.2:c.661G>T | ENSP00000417241.2:p.Ala221Ser | |
| ENST00000470026.6:c.661G>T | ENSP00000419274.2:p.Ala221Ser | |
| ENST00000473961.6:c.545-995G>T | ENSP00000420201.2:n.545-995G>T | |
| ENST00000476777.6:c.658G>T | ENSP00000417554.2:p.Ala220Ser | |
| ENST00000477152.6:c.583G>T | ENSP00000419988.2:p.Ala195Ser | |
| ENST00000478531.6:c.658G>T | ENSP00000420412.2:p.Ala220Ser | |
| ENST00000489037.2:c.583G>T | ENSP00000420781.2:p.Ala195Ser | |
| ENST00000493919.6:c.520G>T | ENSP00000418819.2:p.Ala174Ser | |
| ENST00000494123.6:c.661G>T | ENSP00000419103.2:p.Ala221Ser | |
| ENST00000497488.2:c.-218-995G>T | ENSP00000418986.2:n.-218-995G>T | |
| ENST00000618469.2:c.661G>T | ENSP00000478114.2:p.Ala221Ser | |
| ENST00000634433.2:c.548-995G>T | ENSP00000489431.2:n.548-995G>T | |
| ENST00000644379.2:c.661G>T | ENSP00000496570.2:p.Ala221Ser | |
| ENST00000644555.2:c.520G>T | ENSP00000494614.2:p.Ala174Ser | |
| ENST00000652672.2:c.520G>T | ENSP00000498906.2:p.Ala174Ser | |
| ENST00000484087.6:c.548-995G>T | ENSP00000419481.2:n.548-995G>T | |
| ENST00000700182.1:c.580G>T | ENSP00000514849.1:p.Ala194Ser | |
| ENST00000700183.1:c.*669G>T | ENSP00000514850.1:n.*669G>T | |
| ENST00000357654.9:c.661G>T MANE Select | ENSP00000350283.3:p.Ala221Ser | |
| ENST00000471181.7:c.661G>T | ENSP00000418960.2:p.Ala221Ser | |
| ENST00000642945.1:c.*535G>T | ENSP00000495897.1:n.*535G>T | |
| ENST00000652672.1:c.520G>T | ENSP00000498906.1:p.Ala174Ser | |
| ENST00000352993.7:c.661G>T | ENSP00000312236.5:p.Ala221Ser | |
| ENST00000354071.7:c.661G>T | ENSP00000326002.7:p.Ala221Ser | |
| ENST00000357654.7:c.661G>T | ENSP00000350283.3:p.Ala221Ser | |
| ENST00000412061.3:c.12G>T | ||
| ENST00000461221.5:c.*444G>T | ENSP00000418548.1:n.*444G>T | |
| ENST00000468300.5:c.661G>T | ENSP00000417148.1:p.Ala221Ser | |
| ENST00000470026.5:c.661G>T | ENSP00000419274.1:p.Ala221Ser | |
| ENST00000471181.6:c.661G>T | ENSP00000418960.2:p.Ala221Ser | |
| ENST00000473961.5:c.268-995G>T | ||
| ENST00000476777.5:c.658G>T | ENSP00000417554.1:p.Ala220Ser | |
| ENST00000477152.5:c.583G>T | ENSP00000419988.1:p.Ala195Ser | |
| ENST00000478531.5:c.658G>T | ENSP00000420412.1:p.Ala220Ser | |
| ENST00000484087.5:c.293-995G>T | ENSP00000419481.1:n.293-995G>T | |
| ENST00000487825.5:c.296-995G>T | ENSP00000418212.1:n.296-995G>T | |
| ENST00000491747.6:c.661G>T | ENSP00000420705.2:p.Ala221Ser | |
| ENST00000492859.5:c.*597G>T | ENSP00000420253.1:n.*597G>T | |
| ENST00000493795.5:c.520G>T | ENSP00000418775.1:p.Ala174Ser | |
| ENST00000493919.5:c.520G>T | ENSP00000418819.1:p.Ala174Ser | |
| ENST00000494123.5:c.661G>T | ENSP00000419103.1:p.Ala221Ser | |
| ENST00000497488.1:c.-218-995G>T | ENSP00000418986.1:n.-218-995G>T | |
| ENST00000586385.5:c.4+29327G>T | ENSP00000465818.1:n.4+29327G>T | |
| ENST00000591534.5:c.-43-21334G>T | ENSP00000467329.1:n.-43-21334G>T | |
| ENST00000591849.5:c.-99+29416G>T | ENSP00000465347.1:n.-99+29416G>T | |
| ENST00000634433.1:c.548-995G>T | ENSP00000489431.1:n.548-995G>T | |
| NM_007294.3:c.661G>T , LRG_292t1:c.661G>T | NP_009225.1:p.Ala221Ser | |
| NM_007297.3:c.520G>T | NP_009228.2:p.Ala174Ser | |
| NM_007298.3:c.661G>T | NP_009229.2:p.Ala221Ser | |
| NM_007299.3:c.661G>T | NP_009230.2:p.Ala221Ser | |
| NM_007300.3:c.661G>T | NP_009231.2:p.Ala221Ser | |
| NR_027676.1:n.797G>T | ||
| NM_007294.4:c.661G>T MANE Select | NP_009225.1:p.Ala221Ser | |
| NM_007297.4:c.520G>T | NP_009228.2:p.Ala174Ser | |
| NM_007299.4:c.661G>T | NP_009230.2:p.Ala221Ser | |
| NM_007300.4:c.661G>T | NP_009231.2:p.Ala221Ser | |
| NR_027676.2:n.838G>T |