Linked Data
ClinVar Variation Id:
489476
dbSNP Id:
rs779413228
ExAC:
5:112177527 A / C
gnomAD v2:
5-112177527-A-C
gnomAD v3:
5-112841830-A-C
gnomAD v4:
5-112841830-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112841830A>C , CM000667.2:g.112841830A>C | GRCh38 |
| NC_000005.9:g.112177527A>C , CM000667.1:g.112177527A>C | GRCh37 |
| NC_000005.8:g.112205426A>C | NCBI36 |
| NG_008481.4:g.154310A>C , LRG_130:g.154310A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.6290A>C | ENSP00000473355.2:p.Asp2097Ala | |
| ENST00000505350.2:c.*6242A>C | ENSP00000481752.1:n.*6242A>C | |
| ENST00000507379.6:c.6182A>C | ENSP00000423224.2:p.Asp2061Ala | |
| ENST00000509732.6:c.6236A>C | ENSP00000426541.2:p.Asp2079Ala | |
| ENST00000512211.7:c.6236A>C | ENSP00000423828.3:p.Asp2079Ala | |
| ENST00000257430.9:c.6236A>C MANE Select | ENSP00000257430.4:p.Asp2079Ala | |
| ENST00000257430.8:c.6236A>C | ENSP00000257430.4:p.Asp2079Ala | |
| ENST00000508376.6:c.6236A>C | ENSP00000427089.2:p.Asp2079Ala | |
| ENST00000508624.5:c.*5558A>C | ENSP00000424265.1:n.*5558A>C | |
| ENST00000520401.1:c.230+12858A>C | ||
| NM_000038.5:c.6236A>C | NP_000029.2:p.Asp2079Ala | |
| NM_001127510.2:c.6236A>C | NP_001120982.1:p.Asp2079Ala | |
| NM_001127511.2:c.6182A>C | NP_001120983.2:p.Asp2061Ala | |
| NM_001354895.1:c.6236A>C | NP_001341824.1:p.Asp2079Ala | |
| NM_001354896.1:c.6290A>C | NP_001341825.1:p.Asp2097Ala | |
| NM_001354897.1:c.6266A>C | NP_001341826.1:p.Asp2089Ala | |
| NM_001354898.1:c.6161A>C | NP_001341827.1:p.Asp2054Ala | |
| NM_001354899.1:c.6152A>C | NP_001341828.1:p.Asp2051Ala | |
| NM_001354900.1:c.6113A>C | NP_001341829.1:p.Asp2038Ala | |
| NM_001354901.1:c.6059A>C | NP_001341830.1:p.Asp2020Ala | |
| NM_001354902.1:c.5963A>C | NP_001341831.1:p.Asp1988Ala | |
| NM_001354903.1:c.5933A>C | NP_001341832.1:p.Asp1978Ala | |
| NM_001354904.1:c.5858A>C | NP_001341833.1:p.Asp1953Ala | |
| NM_001354905.1:c.5756A>C | NP_001341834.1:p.Asp1919Ala | |
| NM_001354906.1:c.5387A>C | NP_001341835.1:p.Asp1796Ala | |
| NM_000038.6:c.6236A>C MANE Select | NP_000029.2:p.Asp2079Ala | |
| NM_001127510.3:c.6236A>C | NP_001120982.1:p.Asp2079Ala | |
| NM_001127511.3:c.6182A>C | NP_001120983.2:p.Asp2061Ala | |
| NM_001354895.2:c.6236A>C | NP_001341824.1:p.Asp2079Ala | |
| NM_001354896.2:c.6290A>C | NP_001341825.1:p.Asp2097Ala | |
| NM_001354897.2:c.6266A>C | NP_001341826.1:p.Asp2089Ala | |
| NM_001354898.2:c.6161A>C | NP_001341827.1:p.Asp2054Ala | |
| NM_001354899.2:c.6152A>C | NP_001341828.1:p.Asp2051Ala | |
| NM_001354900.2:c.6113A>C | NP_001341829.1:p.Asp2038Ala | |
| NM_001354901.2:c.6059A>C | NP_001341830.1:p.Asp2020Ala | |
| NM_001354902.2:c.5963A>C | NP_001341831.1:p.Asp1988Ala | |
| NM_001354903.2:c.5933A>C | NP_001341832.1:p.Asp1978Ala | |
| NM_001354904.2:c.5858A>C | NP_001341833.1:p.Asp1953Ala | |
| NM_001354905.2:c.5756A>C | NP_001341834.1:p.Asp1919Ala | |
| NM_001354906.2:c.5387A>C | NP_001341835.1:p.Asp1796Ala |