Linked Data
ClinVar Variation Id:
54860
dbSNP Id:
rs80356867
ExAC:
17:41244181 C / A
gnomAD v2:
17-41244181-C-A
gnomAD v4:
17-43092164-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43092164C>A , CM000679.2:g.43092164C>A | GRCh38 |
| NC_000017.10:g.41244181C>A , CM000679.1:g.41244181C>A | GRCh37 |
| NC_000017.9:g.38497707C>A | NCBI36 |
| NG_005905.2:g.125820G>T , LRG_292:g.125820G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3431G>T | ||
| ENST00000461574.2:c.3367G>T | ENSP00000417241.2:p.Asp1123Tyr | |
| ENST00000470026.6:c.3367G>T | ENSP00000419274.2:p.Asp1123Tyr | |
| ENST00000473961.6:c.3241G>T | ENSP00000420201.2:p.Asp1081Tyr | |
| ENST00000476777.6:c.3364G>T | ENSP00000417554.2:p.Asp1122Tyr | |
| ENST00000477152.6:c.3289G>T | ENSP00000419988.2:p.Asp1097Tyr | |
| ENST00000478531.6:c.785-1132G>T | ENSP00000420412.2:n.785-1132G>T | |
| ENST00000489037.2:c.3289G>T | ENSP00000420781.2:p.Asp1097Tyr | |
| ENST00000493919.6:c.647-1132G>T | ENSP00000418819.2:n.647-1132G>T | |
| ENST00000494123.6:c.3367G>T | ENSP00000419103.2:p.Asp1123Tyr | |
| ENST00000497488.2:c.2479G>T | ENSP00000418986.2:p.Asp827Tyr | |
| ENST00000618469.2:c.3367G>T | ENSP00000478114.2:p.Asp1123Tyr | |
| ENST00000634433.2:c.3244G>T | ENSP00000489431.2:p.Asp1082Tyr | |
| ENST00000644379.2:c.3367G>T | ENSP00000496570.2:p.Asp1123Tyr | |
| ENST00000644555.2:c.647-1132G>T | ENSP00000494614.2:n.647-1132G>T | |
| ENST00000652672.2:c.3226G>T | ENSP00000498906.2:p.Asp1076Tyr | |
| ENST00000484087.6:c.665-1132G>T | ENSP00000419481.2:n.665-1132G>T | |
| ENST00000700182.1:c.707-1132G>T | ENSP00000514849.1:n.707-1132G>T | |
| ENST00000357654.9:c.3367G>T MANE Select | ENSP00000350283.3:p.Asp1123Tyr | |
| ENST00000471181.7:c.3367G>T | ENSP00000418960.2:p.Asp1123Tyr | |
| ENST00000352993.7:c.671-1132G>T | ENSP00000312236.5:n.671-1132G>T | |
| ENST00000354071.7:c.3367G>T | ENSP00000326002.7:p.Asp1123Tyr | |
| ENST00000357654.7:c.3367G>T | ENSP00000350283.3:p.Asp1123Tyr | |
| ENST00000461221.5:c.*3150G>T | ENSP00000418548.1:n.*3150G>T | |
| ENST00000468300.5:c.788-1132G>T | ENSP00000417148.1:n.788-1132G>T | |
| ENST00000471181.6:c.3367G>T | ENSP00000418960.2:p.Asp1123Tyr | |
| ENST00000478531.5:c.785-1132G>T | ENSP00000420412.1:n.785-1132G>T | |
| ENST00000484087.5:c.410-1132G>T | ENSP00000419481.1:n.410-1132G>T | |
| ENST00000487825.5:c.413-1132G>T | ENSP00000418212.1:n.413-1132G>T | |
| ENST00000491747.6:c.788-1132G>T | ENSP00000420705.2:n.788-1132G>T | |
| ENST00000493795.5:c.3226G>T | ENSP00000418775.1:p.Asp1076Tyr | |
| ENST00000493919.5:c.647-1132G>T | ENSP00000418819.1:n.647-1132G>T | |
| ENST00000586385.5:c.5-28213G>T | ENSP00000465818.1:n.5-28213G>T | |
| ENST00000591534.5:c.-43-17643G>T | ENSP00000467329.1:n.-43-17643G>T | |
| ENST00000591849.5:c.-99+33107G>T | ENSP00000465347.1:n.-99+33107G>T | |
| NM_007294.3:c.3367G>T , LRG_292t1:c.3367G>T | NP_009225.1:p.Asp1123Tyr | |
| NM_007297.3:c.3226G>T | NP_009228.2:p.Asp1076Tyr | |
| NM_007298.3:c.788-1132G>T | NP_009229.2:n.788-1132G>T | |
| NM_007299.3:c.788-1132G>T | NP_009230.2:n.788-1132G>T | |
| NM_007300.3:c.3367G>T | NP_009231.2:p.Asp1123Tyr | |
| NR_027676.1:n.3503G>T | ||
| NM_007294.4:c.3367G>T MANE Select | NP_009225.1:p.Asp1123Tyr | |
| NM_007297.4:c.3226G>T | NP_009228.2:p.Asp1076Tyr | |
| NM_007299.4:c.788-1132G>T | NP_009230.2:n.788-1132G>T | |
| NM_007300.4:c.3367G>T | NP_009231.2:p.Asp1123Tyr | |
| NR_027676.2:n.3544G>T |