Linked Data
ClinVar Variation Id:
246510
dbSNP Id:
rs587782173
ExAC:
17:41256884 C / A
gnomAD v2:
17-41256884-C-A
gnomAD v3:
17-43104867-C-A
gnomAD v4:
17-43104867-C-A
PubMed:
PMID:23893897
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43104867C>A , CM000679.2:g.43104867C>A | GRCh38 |
| NC_000017.10:g.41256884C>A , CM000679.1:g.41256884C>A | GRCh37 |
| NC_000017.9:g.38510410C>A | NCBI36 |
| NG_005905.2:g.113117G>T , LRG_292:g.113117G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.365+1G>T | ||
| ENST00000461574.2:c.301+1G>T | ENSP00000417241.2:n.301+1G>T | |
| ENST00000470026.6:c.301+1G>T | ENSP00000419274.2:n.301+1G>T | |
| ENST00000473961.6:c.301+1G>T | ENSP00000420201.2:n.301+1G>T | |
| ENST00000476777.6:c.301+1G>T | ENSP00000417554.2:n.301+1G>T | |
| ENST00000477152.6:c.223+1G>T | ENSP00000419988.2:n.223+1G>T | |
| ENST00000478531.6:c.301+1G>T | ENSP00000420412.2:n.301+1G>T | |
| ENST00000489037.2:c.223+1G>T | ENSP00000420781.2:n.223+1G>T | |
| ENST00000493919.6:c.160+1G>T | ENSP00000418819.2:n.160+1G>T | |
| ENST00000494123.6:c.301+1G>T | ENSP00000419103.2:n.301+1G>T | |
| ENST00000497488.2:c.-218-10007G>T | ENSP00000418986.2:n.-218-10007G>T | |
| ENST00000618469.2:c.301+1G>T | ENSP00000478114.2:n.301+1G>T | |
| ENST00000634433.2:c.301+1G>T | ENSP00000489431.2:n.301+1G>T | |
| ENST00000644379.2:c.301+1G>T | ENSP00000496570.2:n.301+1G>T | |
| ENST00000644555.2:c.160+1G>T | ENSP00000494614.2:n.160+1G>T | |
| ENST00000652672.2:c.160+1G>T | ENSP00000498906.2:n.160+1G>T | |
| ENST00000484087.6:c.301+1G>T | ENSP00000419481.2:n.301+1G>T | |
| ENST00000700083.1:n.1272+1G>T | ||
| ENST00000700182.1:c.223+1G>T | ENSP00000514849.1:n.223+1G>T | |
| ENST00000700183.1:c.*215+1G>T | ENSP00000514850.1:n.*215+1G>T | |
| ENST00000700184.1:n.544+1G>T | ||
| ENST00000357654.9:c.301+1G>T MANE Select | ENSP00000350283.3:n.301+1G>T | |
| ENST00000471181.7:c.301+1G>T | ENSP00000418960.2:n.301+1G>T | |
| ENST00000642945.1:c.*175+1G>T | ENSP00000495897.1:n.*175+1G>T | |
| ENST00000644555.1:c.160+1G>T | ENSP00000494614.1:n.160+1G>T | |
| ENST00000652672.1:c.160+1G>T | ENSP00000498906.1:n.160+1G>T | |
| ENST00000352993.7:c.301+1G>T | ENSP00000312236.5:n.301+1G>T | |
| ENST00000354071.7:c.301+1G>T | ENSP00000326002.7:n.301+1G>T | |
| ENST00000357654.7:c.301+1G>T | ENSP00000350283.3:n.301+1G>T | |
| ENST00000461221.5:c.*87+1G>T | ENSP00000418548.1:n.*87+1G>T | |
| ENST00000461798.5:c.*87+1G>T | ENSP00000417988.1:n.*87+1G>T | |
| ENST00000468300.5:c.301+1G>T | ENSP00000417148.1:n.301+1G>T | |
| ENST00000470026.5:c.301+1G>T | ENSP00000419274.1:n.301+1G>T | |
| ENST00000471181.6:c.301+1G>T | ENSP00000418960.2:n.301+1G>T | |
| ENST00000473961.5:c.24+1G>T | ||
| ENST00000476777.5:c.301+1G>T | ENSP00000417554.1:n.301+1G>T | |
| ENST00000477152.5:c.223+1G>T | ENSP00000419988.1:n.223+1G>T | |
| ENST00000478531.5:c.301+1G>T | ENSP00000420412.1:n.301+1G>T | |
| ENST00000484087.5:c.49+1G>T | ENSP00000419481.1:n.49+1G>T | |
| ENST00000487825.5:c.49+1G>T | ENSP00000418212.1:n.49+1G>T | |
| ENST00000489037.1:c.223+1G>T | ENSP00000420781.1:n.223+1G>T | |
| ENST00000491747.6:c.301+1G>T | ENSP00000420705.2:n.301+1G>T | |
| ENST00000492859.5:c.*237+1G>T | ENSP00000420253.1:n.*237+1G>T | |
| ENST00000493795.5:c.160+1G>T | ENSP00000418775.1:n.160+1G>T | |
| ENST00000493919.5:c.160+1G>T | ENSP00000418819.1:n.160+1G>T | |
| ENST00000494123.5:c.301+1G>T | ENSP00000419103.1:n.301+1G>T | |
| ENST00000497488.1:c.-218-10007G>T | ENSP00000418986.1:n.-218-10007G>T | |
| ENST00000586385.5:c.4+20315G>T | ENSP00000465818.1:n.4+20315G>T | |
| ENST00000591534.5:c.-44+20404G>T | ENSP00000467329.1:n.-44+20404G>T | |
| ENST00000591849.5:c.-99+20404G>T | ENSP00000465347.1:n.-99+20404G>T | |
| ENST00000634433.1:c.301+1G>T | ENSP00000489431.1:n.301+1G>T | |
| NM_007294.3:c.301+1G>T , LRG_292t1:c.301+1G>T | NP_009225.1:n.301+1G>T | |
| NM_007297.3:c.160+1G>T | NP_009228.2:n.160+1G>T | |
| NM_007298.3:c.301+1G>T | NP_009229.2:n.301+1G>T | |
| NM_007299.3:c.301+1G>T | NP_009230.2:n.301+1G>T | |
| NM_007300.3:c.301+1G>T | NP_009231.2:n.301+1G>T | |
| NR_027676.1:n.440+1G>T | ||
| NM_007294.4:c.301+1G>T MANE Select | NP_009225.1:n.301+1G>T | |
| NM_007297.4:c.160+1G>T | NP_009228.2:n.160+1G>T | |
| NM_007299.4:c.301+1G>T | NP_009230.2:n.301+1G>T | |
| NM_007300.4:c.301+1G>T | NP_009231.2:n.301+1G>T | |
| NR_027676.2:n.481+1G>T |