Linked Data
ClinVar Variation Id:
203841
dbSNP Id:
rs148909799
ExAC:
5:7900056 A / G
gnomAD v2:
5-7900056-A-G
gnomAD v3:
5-7899943-A-G
gnomAD v4:
5-7899943-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.7899943A>G , CM000667.2:g.7899943A>G | GRCh38 |
| NC_000005.9:g.7900056A>G , CM000667.1:g.7900056A>G | GRCh37 |
| NC_000005.8:g.7953056A>G | NCBI36 |
| NG_008856.1:g.35840A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000440940.7:c.1982A>G MANE Select | ENSP00000402510.2:p.His661Arg | |
| ENST00000264668.6:c.2063A>G | ENSP00000264668.2:p.His688Arg | |
| ENST00000440940.6:c.1982A>G | ENSP00000402510.2:p.His661Arg | |
| ENST00000506115.1:n.29A>G | ||
| ENST00000510525.5:c.1918A>G | ||
| ENST00000511461.5:c.1895A>G | ||
| ENST00000513439.5:c.*1689A>G | ENSP00000426710.1:n.*1689A>G | |
| NM_002454.2:c.1982A>G | NP_002445.2:p.His661Arg | |
| NM_024010.2:c.2063A>G | NP_076915.2:p.His688Arg | |
| XM_011514044.1:c.1982A>G | XP_011512346.1:p.His661Arg | |
| XR_241703.1:n.1989A>G | ||
| XR_925614.1:n.2108A>G | ||
| NM_001364440.1:c.1982A>G | NP_001351369.1:p.His661Arg | |
| NM_001364441.1:c.1982A>G | NP_001351370.1:p.His661Arg | |
| NM_001364442.1:c.1982A>G | NP_001351371.1:p.His661Arg | |
| NM_024010.3:c.1982A>G | NP_076915.3:p.His661Arg | |
| NR_134480.1:n.2105A>G | ||
| NR_134481.1:n.2030A>G | ||
| NR_134482.1:n.1965A>G | ||
| NR_157168.1:n.2035A>G | ||
| NR_157169.1:n.1895A>G | ||
| NR_157170.1:n.2061A>G | ||
| NR_157171.1:n.1918A>G | ||
| NR_157172.1:n.1832A>G | ||
| NR_157173.1:n.2072A>G | ||
| NR_157174.1:n.2073A>G | ||
| NR_157175.1:n.2227A>G | ||
| NR_157176.1:n.2390A>G | ||
| NR_157177.1:n.2070A>G | ||
| NR_157178.1:n.2098A>G | ||
| XM_024446063.1:c.2027A>G | XP_024301831.1:p.His676Arg | |
| XM_024446064.1:c.1982A>G | XP_024301832.1:p.His661Arg | |
| XR_001742071.1:n.2260A>G | ||
| XR_001742072.1:n.2237A>G | ||
| XR_001742074.1:n.1996A>G | ||
| XR_001742075.1:n.2148A>G | ||
| XR_001742076.1:n.2225A>G | ||
| XR_001742077.1:n.2248A>G | ||
| NM_001364440.2:c.1982A>G | NP_001351369.1:p.His661Arg | |
| NM_001364441.2:c.1982A>G | NP_001351370.1:p.His661Arg | |
| NM_001364442.2:c.1982A>G | NP_001351371.1:p.His661Arg | |
| NM_002454.3:c.1982A>G MANE Select | NP_002445.2:p.His661Arg | |
| NM_024010.4:c.1982A>G | NP_076915.3:p.His661Arg | |
| NR_134480.2:n.2061A>G | ||
| NR_134481.2:n.1986A>G | ||
| NR_134482.2:n.1921A>G | ||
| NR_157168.2:n.2035A>G | ||
| NR_157169.2:n.1895A>G | ||
| NR_157170.2:n.2061A>G | ||
| NR_157171.2:n.1918A>G | ||
| NR_157172.2:n.1832A>G | ||
| NR_157173.2:n.2072A>G | ||
| NR_157174.2:n.2073A>G | ||
| NR_157175.2:n.2227A>G | ||
| NR_157176.2:n.2390A>G | ||
| NR_157177.2:n.2070A>G | ||
| NR_157178.2:n.2098A>G |