Linked Data
ClinVar Variation Id:
468892
dbSNP Id:
rs770781624
ExAC:
1:6530599 C / T
gnomAD v2:
1-6530599-C-T
gnomAD v3:
1-6470539-C-T
gnomAD v4:
1-6470539-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6470539C>T , CM000663.2:g.6470539C>T | GRCh38 |
| NC_000001.10:g.6530599C>T , CM000663.1:g.6530599C>T | GRCh37 |
| NC_000001.9:g.6453186C>T | NCBI36 |
| NG_007978.1:g.54471G>A , LRG_262:g.54471G>A | |
| NG_029910.1:g.657G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340850.10:c.1647G>A | ENSP00000344570.5:p.Glu549= | |
| ENST00000377728.8:c.1647G>A MANE Select | ENSP00000366957.3:p.Glu549= | |
| ENST00000377740.5:c.1647G>A | ENSP00000366969.4:p.Glu549= | |
| ENST00000377748.6:c.1821G>A | ENSP00000366977.2:p.Glu607= | |
| ENST00000400913.6:c.1647G>A | ENSP00000383704.1:p.Glu549= | |
| ENST00000400915.8:c.1758G>A | ENSP00000383706.4:p.Glu586= | |
| ENST00000489097.6:n.2123G>A | ||
| ENST00000535355.6:c.1854G>A | ENSP00000441445.1:p.Glu618= | |
| ENST00000537245.6:c.1758G>A | ENSP00000439625.2:p.Glu586= | |
| ENST00000673471.2:c.1944G>A | ENSP00000500749.1:p.Glu648= | |
| ENST00000674790.1:c.*1859G>A | ENSP00000502815.1:n.*1859G>A | |
| ENST00000674943.1:n.309G>A | ||
| ENST00000675123.1:c.1647G>A | ENSP00000502132.1:p.Glu549= | |
| ENST00000675548.1:c.*1475G>A | ENSP00000502684.1:n.*1475G>A | |
| ENST00000675694.1:c.1647G>A | ENSP00000501925.1:p.Glu549= | |
| ENST00000676401.1:n.194G>A | ||
| ENST00000340850.9:c.1647G>A | ENSP00000344570.5:p.Glu549= | |
| ENST00000377725.5:c.1647G>A | ENSP00000366954.1:p.Glu549= | |
| ENST00000377728.7:c.1647G>A | ENSP00000366957.3:p.Glu549= | |
| ENST00000377732.5:c.1758G>A | ENSP00000366961.1:p.Glu586= | |
| ENST00000377740.4:c.1878G>A | ENSP00000366969.3:p.Glu626= | |
| ENST00000377748.5:c.1878G>A | ENSP00000366977.1:p.Glu626= | |
| ENST00000400913.5:c.1647G>A | ENSP00000383704.1:p.Glu549= | |
| ENST00000400915.7:c.1815G>A | ENSP00000383706.3:p.Glu605= | |
| ENST00000487949.4:n.849G>A | ||
| ENST00000489097.5:n.2123G>A | ||
| ENST00000535355.5:c.1854G>A | ENSP00000441445.1:p.Glu618= | |
| ENST00000537245.5:c.1884G>A | ENSP00000439625.1:p.Glu628= | |
| NM_001042663.1:c.1815G>A | NP_001036128.1:p.Glu605= | |
| NM_001042664.1:c.1647G>A | NP_001036129.1:p.Glu549= | |
| NM_001042665.1:c.1647G>A | NP_001036130.1:p.Glu549= | |
| NM_001265592.1:c.1884G>A | NP_001252521.1:p.Glu628= | |
| NM_001265593.1:c.1854G>A | NP_001252522.1:p.Glu618= | |
| NM_001265594.1:c.1647G>A | NP_001252523.1:p.Glu549= | |
| NM_020631.4:c.1647G>A | NP_065682.2:p.Glu549= | |
| NM_198681.3:c.1878G>A | NP_941374.2:p.Glu626= | |
| NM_001042663.2:c.1815G>A | NP_001036128.1:p.Glu605= | |
| NM_001265594.2:c.1647G>A | NP_001252523.1:p.Glu549= | |
| NM_020631.5:c.1647G>A | NP_065682.2:p.Glu549= | |
| NM_001042663.3:c.1758G>A | NP_001036128.2:p.Glu586= | |
| NM_001265592.2:c.1758G>A | NP_001252521.2:p.Glu586= | |
| NM_020631.6:c.1647G>A MANE Select | NP_065682.2:p.Glu549= | |
| NM_198681.4:c.1647G>A | NP_941374.3:p.Glu549= |