Linked Data
dbSNP Id:
rs774174877
ExAC:
1:55527138 A / G
gnomAD v2:
1-55527138-A-G
gnomAD v4:
1-55061465-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55061465A>G , CM000663.2:g.55061465A>G | GRCh38 |
| NC_000001.10:g.55527138A>G , CM000663.1:g.55527138A>G | GRCh37 |
| NC_000001.9:g.55299726A>G | NCBI36 |
| NG_009061.1:g.26919A>G , LRG_275:g.26919A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.*112A>G | ENSP00000501161.2:n.*112A>G | |
| ENST00000710286.1:c.2129A>G | ENSP00000518176.1:p.His710Arg | |
| ENST00000673903.1:c.1397A>G | ENSP00000501257.1:p.His466Arg | |
| ENST00000673913.1:c.622A>G | ENSP00000501161.1:n.622A>G | |
| ENST00000302118.5:c.1772A>G MANE Select | ENSP00000303208.5:p.His591Arg | |
| ENST00000490692.1:n.2318A>G | ||
| NM_174936.3:c.1772A>G , LRG_275t1:c.1772A>G | NP_777596.2:p.His591Arg | |
| NR_110451.1:n.1379A>G | ||
| XM_011541193.1:c.893A>G | XP_011539495.1:p.His298Arg | |
| NM_174936.4:c.1772A>G MANE Select | NP_777596.2:p.His591Arg | |
| NR_110451.2:n.1379A>G |