Linked Data
dbSNP Id:
rs772711096
ExAC:
4:15591234 C / G
gnomAD v2:
4-15591234-C-G
gnomAD v4:
4-15589611-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.15589611C>G , CM000666.2:g.15589611C>G | GRCh38 |
| NC_000004.11:g.15591234C>G , CM000666.1:g.15591234C>G | GRCh37 |
| NC_000004.10:g.15200332C>G | NCBI36 |
| NG_013035.1:g.124746C>G , LRG_697:g.124746C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389652.11:c.4282C>G | ENSP00000374303.8:p.His1428Asp | |
| ENST00000424120.6:c.4246C>G MANE Select | ENSP00000403465.1:p.His1416Asp | |
| ENST00000503292.6:c.4246C>G | ENSP00000421809.1:p.His1416Asp | |
| ENST00000506643.5:c.4099C>G | ENSP00000422931.2:p.His1367Asp | |
| ENST00000514039.6:c.475C>G | ENSP00000488534.2:p.His159Asp | |
| ENST00000634028.2:c.4099C>G | ENSP00000488669.2:p.His1367Asp | |
| ENST00000650860.2:c.*1743C>G | ENSP00000498775.1:n.*1743C>G | |
| ENST00000674945.1:c.3922C>G | ENSP00000502333.1:p.His1308Asp | |
| ENST00000675768.1:n.1466C>G | ||
| ENST00000680586.1:n.4905C>G | ||
| ENST00000389652.9:c.3744C>G | ||
| ENST00000424120.5:c.4246C>G | ENSP00000403465.1:p.His1416Asp | |
| ENST00000503292.5:c.4246C>G | ENSP00000421809.1:p.His1416Asp | |
| ENST00000506643.4:c.2574C>G | ||
| ENST00000634028.1:c.4052C>G | ENSP00000488669.1:n.4052C>G | |
| NM_001080522.2:c.4246C>G , LRG_697t1:c.4246C>G | NP_001073991.2:p.His1416Asp | |
| XM_005248177.1:c.4246C>G | XP_005248234.1:p.His1416Asp | |
| XM_011513869.1:c.4264C>G | XP_011512171.1:p.His1422Asp | |
| XM_011513870.1:c.4264C>G | XP_011512172.1:p.His1422Asp | |
| XM_011513871.1:c.4117C>G | XP_011512173.1:p.His1373Asp | |
| XM_017008482.1:c.4099C>G | XP_016863971.1:p.His1367Asp | |
| NM_001378615.1:c.4246C>G MANE Select | NP_001365544.1:p.His1416Asp | |
| NM_001378617.1:c.4099C>G | NP_001365546.1:p.His1367Asp |