Linked Data
ClinVar Variation Id:
2143440
ClinVar RCV Id:
RCV003076726
dbSNP Id:
rs748020179
ExAC:
11:71146848 G / A
gnomAD v2:
11-71146848-G-A
gnomAD v4:
11-71435802-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435802G>A , CM000673.2:g.71435802G>A | GRCh38 |
| NC_000011.9:g.71146848G>A , CM000673.1:g.71146848G>A | GRCh37 |
| NC_000011.8:g.70824496G>A | NCBI36 |
| NG_012655.2:g.17630C>T , LRG_340:g.17630C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1001C>T | ENSP00000435707.3:p.Thr334Ile | |
| ENST00000526780.6:c.1001C>T | ENSP00000435668.2:p.Thr334Ile | |
| ENST00000527316.6:c.827C>T | ENSP00000435047.2:p.Thr276Ile | |
| ENST00000682708.1:c.1052C>T | ENSP00000506866.1:p.Thr351Ile | |
| ENST00000683287.1:c.1037C>T | ENSP00000507607.1:p.Thr346Ile | |
| ENST00000683714.1:c.1009C>T | ENSP00000508207.1:p.Pro337Ser | |
| ENST00000684396.1:n.1041C>T | ||
| ENST00000685320.1:c.416C>T | ENSP00000509319.1:p.Thr139Ile | |
| ENST00000690257.1:c.905C>T | ENSP00000510750.1:p.Thr302Ile | |
| ENST00000355527.8:c.1001C>T MANE Select | ENSP00000347717.4:p.Thr334Ile | |
| ENST00000355527.7:c.1001C>T | ENSP00000347717.3:p.Thr334Ile | |
| ENST00000407721.6:c.1001C>T | ENSP00000384739.2:p.Thr334Ile | |
| ENST00000525137.1:c.502C>T | ENSP00000435956.1:p.Pro168Ser | |
| ENST00000533800.5:c.251C>T | ENSP00000435011.1:p.Thr84Ile | |
| ENST00000534795.5:c.319+2010C>T | ||
| NM_001163817.1:c.1001C>T | NP_001157289.1:p.Thr334Ile | |
| NM_001360.2:c.1001C>T , LRG_340t1:c.1001C>T | NP_001351.2:p.Thr334Ile | |
| XM_011544777.1:c.1135C>T | XP_011543079.1:p.Pro379Ser | |
| XM_011544777.2:c.1135C>T | XP_011543079.1:p.Pro379Ser | |
| NM_001163817.2:c.1001C>T | NP_001157289.1:p.Thr334Ile | |
| NM_001360.3:c.1001C>T MANE Select | NP_001351.2:p.Thr334Ile |