Linked Data
ClinVar Variation Id:
37629
dbSNP Id:
rs80358053
gnomAD v2:
17-41219624-C-T
gnomAD v4:
17-43067607-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43067607C>T , CM000679.2:g.43067607C>T | GRCh38 |
| NC_000017.10:g.41219624C>T , CM000679.1:g.41219624C>T | GRCh37 |
| NC_000017.9:g.38473150C>T | NCBI36 |
| NG_005905.2:g.150377G>A , LRG_292:g.150377G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.5071+1G>A | ENSP00000417241.2:n.5071+1G>A | |
| ENST00000470026.6:c.5074+1G>A | ENSP00000419274.2:n.5074+1G>A | |
| ENST00000473961.6:c.4948+1G>A | ENSP00000420201.2:n.4948+1G>A | |
| ENST00000476777.6:c.5068+1G>A | ENSP00000417554.2:n.5068+1G>A | |
| ENST00000477152.6:c.4996+1G>A | ENSP00000419988.2:n.4996+1G>A | |
| ENST00000478531.6:c.1762+1G>A | ENSP00000420412.2:n.1762+1G>A | |
| ENST00000489037.2:c.4996+1G>A | ENSP00000420781.2:n.4996+1G>A | |
| ENST00000493919.6:c.1624+1G>A | ENSP00000418819.2:n.1624+1G>A | |
| ENST00000494123.6:c.5074+1G>A | ENSP00000419103.2:n.5074+1G>A | |
| ENST00000497488.2:c.4186+1G>A | ENSP00000418986.2:n.4186+1G>A | |
| ENST00000618469.2:c.5074+1G>A | ENSP00000478114.2:n.5074+1G>A | |
| ENST00000634433.2:c.4951+1G>A | ENSP00000489431.2:n.4951+1G>A | |
| ENST00000644379.2:c.5140+1G>A | ENSP00000496570.2:n.5140+1G>A | |
| ENST00000644555.2:c.1624+1G>A | ENSP00000494614.2:n.1624+1G>A | |
| ENST00000652672.2:c.4933+1G>A | ENSP00000498906.2:n.4933+1G>A | |
| ENST00000484087.6:c.1636+1G>A | ENSP00000419481.2:n.1636+1G>A | |
| ENST00000357654.9:c.5074+1G>A MANE Select | ENSP00000350283.3:n.5074+1G>A | |
| ENST00000471181.7:c.5137+1G>A | ENSP00000418960.2:n.5137+1G>A | |
| ENST00000644379.1:c.1461+1G>A | ||
| ENST00000352993.7:c.1648+1G>A | ENSP00000312236.5:n.1648+1G>A | |
| ENST00000357654.7:c.5074+1G>A | ENSP00000350283.3:n.5074+1G>A | |
| ENST00000461221.5:c.*4857+1G>A | ENSP00000418548.1:n.*4857+1G>A | |
| ENST00000468300.5:c.1762+1G>A | ENSP00000417148.1:n.1762+1G>A | |
| ENST00000471181.6:c.5137+1G>A | ENSP00000418960.2:n.5137+1G>A | |
| ENST00000472490.1:n.228G>A | ||
| ENST00000478531.5:c.1762+1G>A | ENSP00000420412.1:n.1762+1G>A | |
| ENST00000484087.5:c.1387+1G>A | ENSP00000419481.1:n.1387+1G>A | |
| ENST00000491747.6:c.1762+1G>A | ENSP00000420705.2:n.1762+1G>A | |
| ENST00000493795.5:c.4933+1G>A | ENSP00000418775.1:n.4933+1G>A | |
| ENST00000493919.5:c.1624+1G>A | ENSP00000418819.1:n.1624+1G>A | |
| ENST00000586385.5:c.5-3656G>A | ENSP00000465818.1:n.5-3656G>A | |
| ENST00000591534.5:c.547+1G>A | ENSP00000467329.1:n.547+1G>A | |
| ENST00000591849.5:c.-98-17417G>A | ENSP00000465347.1:n.-98-17417G>A | |
| NM_007294.3:c.5074+1G>A , LRG_292t1:c.5074+1G>A | NP_009225.1:n.5074+1G>A | |
| NM_007297.3:c.4933+1G>A | NP_009228.2:n.4933+1G>A | |
| NM_007298.3:c.1762+1G>A | NP_009229.2:n.1762+1G>A | |
| NM_007299.3:c.1762+1G>A | NP_009230.2:n.1762+1G>A | |
| NM_007300.3:c.5137+1G>A | NP_009231.2:n.5137+1G>A | |
| NR_027676.1:n.5210+1G>A | ||
| NM_007294.4:c.5074+1G>A MANE Select | NP_009225.1:n.5074+1G>A | |
| NM_007297.4:c.4933+1G>A | NP_009228.2:n.4933+1G>A | |
| NM_007299.4:c.1762+1G>A | NP_009230.2:n.1762+1G>A | |
| NM_007300.4:c.5137+1G>A | NP_009231.2:n.5137+1G>A | |
| NR_027676.2:n.5251+1G>A |