Linked Data
ClinVar Variation Id:
482344
dbSNP Id:
rs1554087886
gnomAD v3:
5-112842568-G-A
gnomAD v4:
5-112842568-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112842568G>A , CM000667.2:g.112842568G>A | GRCh38 |
| NC_000005.9:g.112178265G>A , CM000667.1:g.112178265G>A | GRCh37 |
| NC_000005.8:g.112206164G>A | NCBI36 |
| NG_008481.4:g.155048G>A , LRG_130:g.155048G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.7028G>A | ENSP00000473355.2:p.Gly2343Asp | |
| ENST00000505350.2:c.*6980G>A | ENSP00000481752.1:n.*6980G>A | |
| ENST00000507379.6:c.6920G>A | ENSP00000423224.2:p.Gly2307Asp | |
| ENST00000509732.6:c.6974G>A | ENSP00000426541.2:p.Gly2325Asp | |
| ENST00000512211.7:c.6974G>A | ENSP00000423828.3:p.Gly2325Asp | |
| ENST00000257430.9:c.6974G>A MANE Select | ENSP00000257430.4:p.Gly2325Asp | |
| ENST00000257430.8:c.6974G>A | ENSP00000257430.4:p.Gly2325Asp | |
| ENST00000508376.6:c.6974G>A | ENSP00000427089.2:p.Gly2325Asp | |
| ENST00000508624.5:c.*6296G>A | ENSP00000424265.1:n.*6296G>A | |
| ENST00000520401.1:c.230+13596G>A | ||
| NM_000038.5:c.6974G>A | NP_000029.2:p.Gly2325Asp | |
| NM_001127510.2:c.6974G>A | NP_001120982.1:p.Gly2325Asp | |
| NM_001127511.2:c.6920G>A | NP_001120983.2:p.Gly2307Asp | |
| NM_001354895.1:c.6974G>A | NP_001341824.1:p.Gly2325Asp | |
| NM_001354896.1:c.7028G>A | NP_001341825.1:p.Gly2343Asp | |
| NM_001354897.1:c.7004G>A | NP_001341826.1:p.Gly2335Asp | |
| NM_001354898.1:c.6899G>A | NP_001341827.1:p.Gly2300Asp | |
| NM_001354899.1:c.6890G>A | NP_001341828.1:p.Gly2297Asp | |
| NM_001354900.1:c.6851G>A | NP_001341829.1:p.Gly2284Asp | |
| NM_001354901.1:c.6797G>A | NP_001341830.1:p.Gly2266Asp | |
| NM_001354902.1:c.6701G>A | NP_001341831.1:p.Gly2234Asp | |
| NM_001354903.1:c.6671G>A | NP_001341832.1:p.Gly2224Asp | |
| NM_001354904.1:c.6596G>A | NP_001341833.1:p.Gly2199Asp | |
| NM_001354905.1:c.6494G>A | NP_001341834.1:p.Gly2165Asp | |
| NM_001354906.1:c.6125G>A | NP_001341835.1:p.Gly2042Asp | |
| NM_000038.6:c.6974G>A MANE Select | NP_000029.2:p.Gly2325Asp | |
| NM_001127510.3:c.6974G>A | NP_001120982.1:p.Gly2325Asp | |
| NM_001127511.3:c.6920G>A | NP_001120983.2:p.Gly2307Asp | |
| NM_001354895.2:c.6974G>A | NP_001341824.1:p.Gly2325Asp | |
| NM_001354896.2:c.7028G>A | NP_001341825.1:p.Gly2343Asp | |
| NM_001354897.2:c.7004G>A | NP_001341826.1:p.Gly2335Asp | |
| NM_001354898.2:c.6899G>A | NP_001341827.1:p.Gly2300Asp | |
| NM_001354899.2:c.6890G>A | NP_001341828.1:p.Gly2297Asp | |
| NM_001354900.2:c.6851G>A | NP_001341829.1:p.Gly2284Asp | |
| NM_001354901.2:c.6797G>A | NP_001341830.1:p.Gly2266Asp | |
| NM_001354902.2:c.6701G>A | NP_001341831.1:p.Gly2234Asp | |
| NM_001354903.2:c.6671G>A | NP_001341832.1:p.Gly2224Asp | |
| NM_001354904.2:c.6596G>A | NP_001341833.1:p.Gly2199Asp | |
| NM_001354905.2:c.6494G>A | NP_001341834.1:p.Gly2165Asp | |
| NM_001354906.2:c.6125G>A | NP_001341835.1:p.Gly2042Asp |