Linked Data
ClinVar Variation Id:
753319
ClinVar RCV Id:
RCV001465418
dbSNP Id:
rs1593072345
MyVariant Identifiers:
chr12:g.133249813G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.132673227G>A , CM000674.2:g.132673227G>A | GRCh38 |
| NC_000012.11:g.133249813G>A , CM000674.1:g.133249813G>A | GRCh37 |
| NC_000012.10:g.131759886G>A | NCBI36 |
| NG_033840.1:g.19298C>T , LRG_789:g.19298C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539215.6:c.118C>T | ||
| ENST00000545015.2:n.1437C>T | ||
| ENST00000699982.1:c.1264C>T | ||
| ENST00000699983.1:c.1264C>T | ||
| ENST00000699984.1:c.1264C>T | ||
| ENST00000320574.10:c.1410C>T MANE Select | ENSP00000322570.5:p.Tyr470= | |
| ENST00000672742.1:c.*912C>T | ENSP00000500279.1:n.*912C>T | |
| ENST00000320574.9:c.1410C>T | ENSP00000322570.5:p.Tyr470= | |
| ENST00000535270.5:c.1329C>T | ENSP00000445753.1:p.Tyr443= | |
| ENST00000535934.2:n.1285C>T | ||
| ENST00000537064.5:c.*457C>T | ENSP00000442578.1:n.*457C>T | |
| ENST00000539215.5:n.118C>T | ||
| ENST00000545015.1:n.7C>T | ||
| NM_006231.3:c.1410C>T , LRG_789t1:c.1410C>T | NP_006222.2:p.Tyr470= | |
| XM_011534795.1:c.1410C>T | XP_011533097.1:p.Tyr470= | |
| XM_011534796.1:c.1281C>T | XP_011533098.1:p.Tyr427= | |
| XM_011534797.1:c.489C>T | XP_011533099.1:p.Tyr163= | |
| XM_011534798.1:c.72C>T | XP_011533100.1:p.Tyr24= | |
| XM_011534799.1:c.1410C>T | XP_011533101.1:p.Tyr470= | |
| XM_011534800.1:c.1410C>T | XP_011533102.1:p.Tyr470= | |
| XM_011534801.1:c.1410C>T | XP_011533103.1:p.Tyr470= | |
| XR_941395.1:n.1619C>T | ||
| XM_011534795.3:c.1410C>T | XP_011533097.1:p.Tyr470= | |
| XM_011534797.3:c.489C>T | XP_011533099.1:p.Tyr163= | |
| XM_011534799.2:c.1410C>T | XP_011533101.1:p.Tyr470= | |
| XR_002957338.1:n.1614C>T | ||
| XR_002957339.1:n.1614C>T | ||
| XR_941395.2:n.1614C>T | ||
| NM_006231.4:c.1410C>T MANE Select | NP_006222.2:p.Tyr470= |