Linked Data
ClinVar Variation Id:
1926178
ClinVar RCV Id:
RCV002626281
dbSNP Id:
rs760887459
ExAC:
11:71155093 A / G
gnomAD v2:
11-71155093-A-G
gnomAD v3:
11-71444047-A-G
gnomAD v4:
11-71444047-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71444047A>G , CM000673.2:g.71444047A>G | GRCh38 |
| NC_000011.9:g.71155093A>G , CM000673.1:g.71155093A>G | GRCh37 |
| NC_000011.8:g.70832741A>G | NCBI36 |
| NG_012655.2:g.9385T>C , LRG_340:g.9385T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.267T>C | ENSP00000435707.3:p.Thr89= | |
| ENST00000526780.6:c.267T>C | ENSP00000435668.2:p.Thr89= | |
| ENST00000527316.6:c.93T>C | ENSP00000435047.2:p.Thr31= | |
| ENST00000529990.6:c.93T>C | ENSP00000435058.2:p.Thr31= | |
| ENST00000682708.1:c.267T>C | ENSP00000506866.1:p.Thr89= | |
| ENST00000682880.1:c.267T>C | ENSP00000507520.1:p.Thr89= | |
| ENST00000683287.1:c.267T>C | ENSP00000507607.1:p.Thr89= | |
| ENST00000683714.1:c.267T>C | ENSP00000508207.1:p.Thr89= | |
| ENST00000683874.1:n.544T>C | ||
| ENST00000685320.1:c.-319T>C | ENSP00000509319.1:n.-319T>C | |
| ENST00000690257.1:c.171T>C | ENSP00000510750.1:p.Thr57= | |
| ENST00000355527.8:c.267T>C MANE Select | ENSP00000347717.4:p.Thr89= | |
| ENST00000355527.7:c.267T>C | ENSP00000347717.3:p.Thr89= | |
| ENST00000407721.6:c.267T>C | ENSP00000384739.2:p.Thr89= | |
| ENST00000525346.5:c.267T>C | ENSP00000435707.2:p.Thr89= | |
| ENST00000526780.5:c.267T>C | ENSP00000435668.1:p.Thr89= | |
| ENST00000527316.5:c.171T>C | ENSP00000435047.1:p.Thr57= | |
| ENST00000527452.1:c.267T>C | ENSP00000436007.1:p.Thr89= | |
| ENST00000529990.5:c.207T>C | ENSP00000435058.1:p.Thr69= | |
| ENST00000531364.5:c.267T>C | ENSP00000432589.1:p.Thr89= | |
| NM_001163817.1:c.267T>C | NP_001157289.1:p.Thr89= | |
| NM_001360.2:c.267T>C , LRG_340t1:c.267T>C | NP_001351.2:p.Thr89= | |
| XM_011544777.1:c.267T>C | XP_011543079.1:p.Thr89= | |
| XM_011544777.2:c.267T>C | XP_011543079.1:p.Thr89= | |
| NM_001163817.2:c.267T>C | NP_001157289.1:p.Thr89= | |
| NM_001360.3:c.267T>C MANE Select | NP_001351.2:p.Thr89= |