Linked Data
ClinVar Variation Id:
1549609
ClinVar RCV Id:
RCV002182810
dbSNP Id:
rs762215750
ExAC:
11:71146889 G / A
gnomAD v2:
11-71146889-G-A
gnomAD v4:
11-71435843-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435843G>A , CM000673.2:g.71435843G>A | GRCh38 |
| NC_000011.9:g.71146889G>A , CM000673.1:g.71146889G>A | GRCh37 |
| NC_000011.8:g.70824537G>A | NCBI36 |
| NG_012655.2:g.17589C>T , LRG_340:g.17589C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.964-4C>T | ENSP00000435707.3:n.964-4C>T | |
| ENST00000526780.6:c.964-4C>T | ENSP00000435668.2:n.964-4C>T | |
| ENST00000527316.6:c.790-4C>T | ENSP00000435047.2:n.790-4C>T | |
| ENST00000682708.1:c.1015-4C>T | ENSP00000506866.1:n.1015-4C>T | |
| ENST00000683287.1:c.1000-4C>T | ENSP00000507607.1:n.1000-4C>T | |
| ENST00000683714.1:c.972-4C>T | ENSP00000508207.1:n.972-4C>T | |
| ENST00000684396.1:n.1004-4C>T | ||
| ENST00000685320.1:c.379-4C>T | ENSP00000509319.1:n.379-4C>T | |
| ENST00000690257.1:c.868-4C>T | ENSP00000510750.1:n.868-4C>T | |
| ENST00000355527.8:c.964-4C>T MANE Select | ENSP00000347717.4:n.964-4C>T | |
| ENST00000355527.7:c.964-4C>T | ENSP00000347717.3:n.964-4C>T | |
| ENST00000407721.6:c.964-4C>T | ENSP00000384739.2:n.964-4C>T | |
| ENST00000525137.1:c.461C>T | ENSP00000435956.1:p.Pro154Leu | |
| ENST00000533800.5:c.214-4C>T | ENSP00000435011.1:n.214-4C>T | |
| ENST00000534795.5:c.319+1969C>T | ||
| NM_001163817.1:c.964-4C>T | NP_001157289.1:n.964-4C>T | |
| NM_001360.2:c.964-4C>T , LRG_340t1:c.964-4C>T | NP_001351.2:n.964-4C>T | |
| XM_011544777.1:c.1094C>T | XP_011543079.1:p.Pro365Leu | |
| XM_011544777.2:c.1094C>T | XP_011543079.1:p.Pro365Leu | |
| NM_001163817.2:c.964-4C>T | NP_001157289.1:n.964-4C>T | |
| NM_001360.3:c.964-4C>T MANE Select | NP_001351.2:n.964-4C>T |