Linked Data
ClinVar Variation Id:
458678
dbSNP Id:
rs1173707321
gnomAD v2:
11-71146879-A-G
gnomAD v4:
11-71435833-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435833A>G , CM000673.2:g.71435833A>G | GRCh38 |
| NC_000011.9:g.71146879A>G , CM000673.1:g.71146879A>G | GRCh37 |
| NC_000011.8:g.70824527A>G | NCBI36 |
| NG_012655.2:g.17599T>C , LRG_340:g.17599T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.970T>C | ENSP00000435707.3:p.Tyr324His | |
| ENST00000526780.6:c.970T>C | ENSP00000435668.2:p.Tyr324His | |
| ENST00000527316.6:c.796T>C | ENSP00000435047.2:p.Tyr266His | |
| ENST00000682708.1:c.1021T>C | ENSP00000506866.1:p.Tyr341His | |
| ENST00000683287.1:c.1006T>C | ENSP00000507607.1:p.Tyr336His | |
| ENST00000683714.1:c.978T>C | ENSP00000508207.1:p.Cys326= | |
| ENST00000684396.1:n.1010T>C | ||
| ENST00000685320.1:c.385T>C | ENSP00000509319.1:p.Tyr129His | |
| ENST00000690257.1:c.874T>C | ENSP00000510750.1:p.Tyr292His | |
| ENST00000355527.8:c.970T>C MANE Select | ENSP00000347717.4:p.Tyr324His | |
| ENST00000355527.7:c.970T>C | ENSP00000347717.3:p.Tyr324His | |
| ENST00000407721.6:c.970T>C | ENSP00000384739.2:p.Tyr324His | |
| ENST00000525137.1:c.471T>C | ENSP00000435956.1:p.Cys157= | |
| ENST00000533800.5:c.220T>C | ENSP00000435011.1:p.Tyr74His | |
| ENST00000534795.5:c.319+1979T>C | ||
| NM_001163817.1:c.970T>C | NP_001157289.1:p.Tyr324His | |
| NM_001360.2:c.970T>C , LRG_340t1:c.970T>C | NP_001351.2:p.Tyr324His | |
| XM_011544777.1:c.1104T>C | XP_011543079.1:p.Cys368= | |
| XM_011544777.2:c.1104T>C | XP_011543079.1:p.Cys368= | |
| NM_001163817.2:c.970T>C | NP_001157289.1:p.Tyr324His | |
| NM_001360.3:c.970T>C MANE Select | NP_001351.2:p.Tyr324His |