Linked Data
ClinVar Variation Id:
255831
dbSNP Id:
rs886038281
gnomAD v3:
X-38298950-T-C
gnomAD v4:
X-38298950-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38298950T>C , CM000685.2:g.38298950T>C | GRCh38 |
| NC_000023.10:g.38158203T>C , CM000685.1:g.38158203T>C | GRCh37 |
| NC_000023.9:g.38043147T>C | NCBI36 |
| NG_009553.1:g.33586A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494707.6:c.449+6A>G | ||
| ENST00000642170.1:n.1499+6A>G | ||
| ENST00000642395.2:c.1245+6A>G | ENSP00000493468.2:n.1245+6A>G | |
| ENST00000642739.1:c.1245+6A>G | ENSP00000493596.1:n.1245+6A>G | |
| ENST00000644238.1:c.1060-1498A>G | ENSP00000496728.1:n.1060-1498A>G | |
| ENST00000644337.1:c.1060-1498A>G | ENSP00000494557.1:n.1060-1498A>G | |
| ENST00000645032.1:c.1245+6A>G MANE Select | ENSP00000495537.1:n.1245+6A>G | |
| ENST00000645124.1:c.1245+6A>G | ENSP00000496446.1:n.1245+6A>G | |
| ENST00000646020.1:c.1305+6A>G | ENSP00000494745.1:n.1305+6A>G | |
| ENST00000318842.11:c.1245+6A>G | ENSP00000322219.6:n.1245+6A>G | |
| ENST00000339363.7:c.1245+6A>G | ENSP00000343671.3:n.1245+6A>G | |
| ENST00000378505.6:c.1245+6A>G | ENSP00000367766.2:n.1245+6A>G | |
| ENST00000464437.1:c.311+6A>G | ||
| ENST00000465127.1:c.172-367171T>C | ENSP00000417050.1:n.172-367171T>C | |
| ENST00000474584.5:c.1245+6A>G | ENSP00000418926.1:n.1245+6A>G | |
| ENST00000482855.5:c.1245+6A>G | ENSP00000419276.1:n.1245+6A>G | |
| ENST00000494841.1:n.508+6A>G | ||
| NM_000328.2:c.1245+6A>G | NP_000319.1:n.1245+6A>G | |
| NM_001034853.1:c.1245+6A>G | NP_001030025.1:n.1245+6A>G | |
| XM_005272633.1:c.1245+6A>G | XP_005272690.1:n.1245+6A>G | |
| XM_011543940.1:c.1242+6A>G | XP_011542242.1:n.1242+6A>G | |
| XM_005272633.3:c.1245+6A>G | XP_005272690.1:n.1245+6A>G | |
| XM_011543940.3:c.1242+6A>G | XP_011542242.1:n.1242+6A>G | |
| XM_017029712.2:c.1242+6A>G | XP_016885201.1:n.1242+6A>G | |
| NM_001367245.1:c.1242+6A>G | NP_001354174.1:n.1242+6A>G | |
| NM_001367246.1:c.1060-1498A>G | NP_001354175.1:n.1060-1498A>G | |
| NM_001367247.1:c.1245+6A>G | NP_001354176.1:n.1245+6A>G | |
| NM_001367248.1:c.1275+6A>G | NP_001354177.1:n.1275+6A>G | |
| NM_001367249.1:c.1242+6A>G | NP_001354178.1:n.1242+6A>G | |
| NM_001367250.1:c.1242+6A>G | NP_001354179.1:n.1242+6A>G | |
| NM_001367251.1:c.1060-1498A>G | NP_001354180.1:n.1060-1498A>G | |
| NR_159803.1:n.1447+6A>G | ||
| NR_159804.1:n.1296+6A>G | ||
| NR_159805.1:n.1387+6A>G | ||
| NR_159806.1:n.1387+6A>G | ||
| NR_159807.1:n.1387+6A>G | ||
| NR_159808.1:n.1499+6A>G | ||
| NM_000328.3:c.1245+6A>G | NP_000319.1:n.1245+6A>G | |
| NM_001034853.2:c.1245+6A>G MANE Select | NP_001030025.1:n.1245+6A>G |