Linked Data
ClinVar Variation Id:
375761
ClinVar RCV Id:
RCV000417236
dbSNP Id:
rs1057519640
gnomAD v2:
18-2697032-A-G
gnomAD v4:
18-2697034-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.2697034A>G , CM000680.2:g.2697034A>G | GRCh38 |
| NC_000018.9:g.2697032A>G , CM000680.1:g.2697032A>G | GRCh37 |
| NC_000018.8:g.2687032A>G | NCBI36 |
| NG_031972.1:g.46147A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684915.1:n.1200A>G | ||
| ENST00000688342.1:c.1043A>G | ENSP00000508422.1:p.His348Arg | |
| ENST00000693213.1:n.321A>G | ||
| ENST00000320876.11:c.1043A>G MANE Select | ENSP00000326603.7:p.His348Arg | |
| ENST00000320876.10:c.1043A>G | ENSP00000326603.6:p.His348Arg | |
| ENST00000581226.1:n.277A>G | ||
| NM_015295.2:c.1043A>G | NP_056110.2:p.His348Arg | |
| XM_011525642.1:c.1043A>G | XP_011523944.1:p.His348Arg | |
| XM_011525643.1:c.1043A>G | XP_011523945.1:p.His348Arg | |
| XM_011525644.1:c.659A>G | XP_011523946.1:p.His220Arg | |
| XM_011525645.1:c.479A>G | XP_011523947.1:p.His160Arg | |
| XM_011525646.1:c.1043A>G | XP_011523948.1:p.His348Arg | |
| XM_011525647.1:c.1043A>G | XP_011523949.1:p.His348Arg | |
| XR_430039.1:n.1232A>G | ||
| XR_935054.1:n.1232A>G | ||
| XR_935055.1:n.1232A>G | ||
| XM_011525643.2:c.1043A>G | XP_011523945.1:p.His348Arg | |
| XM_017025684.1:c.479A>G | XP_016881173.1:p.His160Arg | |
| XR_001753172.1:n.1232A>G | ||
| XR_001753173.1:n.1232A>G | ||
| XR_001753174.1:n.1232A>G | ||
| XR_001753175.1:n.1232A>G | ||
| XR_001753176.1:n.1232A>G | ||
| XR_001753177.1:n.1232A>G | ||
| XR_001753178.1:n.1232A>G | ||
| XR_001753179.1:n.1232A>G | ||
| XR_935055.2:n.1232A>G | ||
| NM_015295.3:c.1043A>G MANE Select | NP_056110.2:p.His348Arg |