Linked Data
dbSNP Id:
rs11700462
gnomAD v2:
21-38817812-G-A
gnomAD v3:
21-37445510-G-A
gnomAD v4:
21-37445510-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.37445510G>A , CM000683.2:g.37445510G>A | GRCh38 |
| NC_000021.8:g.38817812G>A , CM000683.1:g.38817812G>A | GRCh37 |
| NC_000021.7:g.37739682G>A | NCBI36 |
| NG_009366.1:g.82954G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000338785.8:c.10+25126G>A | ENSP00000342690.3:n.10+25126G>A | |
| ENST00000398960.7:c.10+25126G>A | ENSP00000381932.2:n.10+25126G>A | |
| ENST00000426672.6:c.10+25126G>A | ENSP00000412269.2:n.10+25126G>A | |
| ENST00000455097.6:c.-78+15110G>A | ENSP00000398483.2:n.-78+15110G>A | |
| ENST00000642309.1:c.-78+15110G>A | ENSP00000495596.1:n.-78+15110G>A | |
| ENST00000643551.1:c.10+25126G>A | ENSP00000494698.1:n.10+25126G>A | |
| ENST00000643624.1:c.10+25126G>A | ENSP00000493627.1:n.10+25126G>A | |
| ENST00000643854.1:c.-78+23644G>A | ENSP00000493653.1:n.-78+23644G>A | |
| ENST00000644942.1:c.10+25126G>A | ENSP00000494544.1:n.10+25126G>A | |
| ENST00000645424.1:c.10+25126G>A | ENSP00000494897.1:n.10+25126G>A | |
| ENST00000645774.1:c.-148-10620G>A | ENSP00000494536.1:n.-148-10620G>A | |
| ENST00000646523.1:c.10+25126G>A | ENSP00000495632.1:n.10+25126G>A | |
| ENST00000646548.1:c.10+25126G>A | ENSP00000495908.1:n.10+25126G>A | |
| ENST00000647188.2:c.10+25126G>A MANE Select | ENSP00000494572.1:n.10+25126G>A | |
| ENST00000647425.1:c.10+25126G>A | ENSP00000496748.1:n.10+25126G>A | |
| ENST00000647504.1:c.-77-27174G>A | ENSP00000495571.1:n.-77-27174G>A | |
| ENST00000338785.7:c.10+25126G>A | ENSP00000342690.3:n.10+25126G>A | |
| ENST00000339659.8:c.10+25126G>A | ENSP00000340373.3:n.10+25126G>A | |
| ENST00000398956.2:c.10+25126G>A | ENSP00000381929.2:n.10+25126G>A | |
| ENST00000398960.6:c.10+25126G>A | ENSP00000381932.2:n.10+25126G>A | |
| ENST00000426672.5:c.10+25126G>A | ENSP00000412269.1:n.10+25126G>A | |
| ENST00000455097.5:c.10+25126G>A | ENSP00000398483.1:n.10+25126G>A | |
| ENST00000462274.1:n.696-27174G>A | ||
| ENST00000498351.1:n.192+15110G>A | ||
| NM_001396.3:c.10+25126G>A | NP_001387.2:n.10+25126G>A | |
| NM_101395.2:c.10+25126G>A | NP_567824.1:n.10+25126G>A | |
| NM_130436.2:c.10+25126G>A | NP_569120.1:n.10+25126G>A | |
| NM_130438.2:c.10+25126G>A | NP_569122.1:n.10+25126G>A | |
| XM_005260931.3:c.-78+15110G>A | XP_005260988.1:n.-78+15110G>A | |
| XM_006723976.2:c.10+25126G>A | XP_006724039.1:n.10+25126G>A | |
| XM_006723977.2:c.10+25126G>A | XP_006724040.1:n.10+25126G>A | |
| XM_006723978.2:c.10+25126G>A | XP_006724041.1:n.10+25126G>A | |
| XM_006723979.2:c.10+25126G>A | XP_006724042.1:n.10+25126G>A | |
| XM_011529483.1:c.10+25126G>A | XP_011527785.1:n.10+25126G>A | |
| XM_011529485.1:c.-77-27174G>A | XP_011527787.1:n.-77-27174G>A | |
| NM_001347721.1:c.10+25126G>A | NP_001334650.1:n.10+25126G>A | |
| NM_001347722.1:c.10+25126G>A | NP_001334651.1:n.10+25126G>A | |
| NM_001347723.1:c.-77-27174G>A | NP_001334652.1:n.-77-27174G>A | |
| NM_001396.4:c.10+25126G>A | NP_001387.2:n.10+25126G>A | |
| XM_006723976.3:c.10+25126G>A | XP_006724039.1:n.10+25126G>A | |
| XM_006723977.3:c.10+25126G>A | XP_006724040.1:n.10+25126G>A | |
| XM_006723978.3:c.10+25126G>A | XP_006724041.1:n.10+25126G>A | |
| XM_011529483.2:c.10+25126G>A | XP_011527785.1:n.10+25126G>A | |
| XM_017028284.1:c.10+25126G>A | XP_016883773.1:n.10+25126G>A | |
| XM_017028286.2:c.-78+15110G>A | XP_016883775.1:n.-78+15110G>A | |
| XM_024452057.1:c.-78+15110G>A | XP_024307825.1:n.-78+15110G>A | |
| NM_001347721.2:c.10+25126G>A MANE Select | NP_001334650.1:n.10+25126G>A | |
| NM_001347722.2:c.10+25126G>A | NP_001334651.1:n.10+25126G>A | |
| NM_001347723.2:c.-77-27174G>A | NP_001334652.1:n.-77-27174G>A | |
| NM_001396.5:c.10+25126G>A | NP_001387.2:n.10+25126G>A |