Linked Data
ClinVar Variation Id:
527671
ClinVar RCV Id:
RCV002377364
dbSNP Id:
rs1060500385
gnomAD v2:
17-29676262-C-T
gnomAD v3:
17-31349244-C-T
gnomAD v4:
17-31349244-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31349244C>T , CM000679.2:g.31349244C>T | GRCh38 |
| NC_000017.10:g.29676262C>T , CM000679.1:g.29676262C>T | GRCh37 |
| NC_000017.9:g.26700388C>T | NCBI36 |
| NG_009018.1:g.259268C>T , LRG_214:g.259268C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696138.1:c.7296C>T | ENSP00000512431.1:p.Tyr2432= | |
| ENST00000684826.1:c.1878C>T | ENSP00000509994.1:p.Tyr626= | |
| ENST00000687027.1:c.1470C>T | ENSP00000508715.1:p.Tyr490= | |
| ENST00000687863.1:n.3959C>T | ||
| ENST00000689464.1:c.364C>T | ||
| ENST00000691014.1:c.7344C>T | ENSP00000510595.1:p.Tyr2448= | |
| ENST00000693617.1:c.1878C>T | ENSP00000510031.1:p.Tyr626= | |
| ENST00000358273.9:c.7314C>T MANE Select | ENSP00000351015.4:p.Tyr2438= | |
| ENST00000356175.7:c.7251C>T | ENSP00000348498.3:p.Tyr2417= | |
| ENST00000358273.8:c.7314C>T | ENSP00000351015.4:p.Tyr2438= | |
| ENST00000456735.6:c.6249C>T | ENSP00000389907.2:p.Tyr2083= | |
| ENST00000471572.6:c.697C>T | ||
| ENST00000579081.5:c.7450C>T | ENSP00000462408.1:n.7450C>T | |
| ENST00000581790.5:c.457C>T | ||
| NM_000267.3:c.7251C>T , LRG_214t1:c.7251C>T | NP_000258.1:p.Tyr2417= | |
| NM_001042492.2:c.7314C>T , LRG_214t2:c.7314C>T | NP_001035957.1:p.Tyr2438= | |
| XM_005257983.1:c.7314C>T | XP_005258040.1:p.Tyr2438= | |
| XM_005257984.1:c.7251C>T | XP_005258041.1:p.Tyr2417= | |
| XM_006721922.1:c.7344C>T | XP_006721985.1:p.Tyr2448= | |
| XM_006721923.2:c.7305C>T | XP_006721986.1:p.Tyr2435= | |
| XM_006721924.1:c.7344C>T | XP_006721987.1:p.Tyr2448= | |
| XM_006721925.1:c.7281C>T | XP_006721988.1:p.Tyr2427= | |
| XM_006721926.2:c.7344C>T | XP_006721989.1:p.Tyr2448= | |
| XM_006721927.1:c.7344C>T | XP_006721990.1:p.Tyr2448= | |
| XM_011524852.1:c.7341C>T | XP_011523154.1:p.Tyr2447= | |
| XM_011524853.1:c.7305C>T | XP_011523155.1:p.Tyr2435= | |
| XM_011524854.1:c.7305C>T | XP_011523156.1:p.Tyr2435= | |
| XM_011524855.1:c.7305C>T | XP_011523157.1:p.Tyr2435= | |
| XM_011524856.1:c.7305C>T | XP_011523158.1:p.Tyr2435= | |
| XM_011524857.1:c.7344C>T | XP_011523159.1:p.Tyr2448= | |
| NM_001042492.3:c.7314C>T MANE Select | NP_001035957.1:p.Tyr2438= |