Linked Data
ClinVar Variation Id:
96648
dbSNP Id:
rs145007686
ExAC:
7:33312692 A / G
gnomAD v2:
7-33312692-A-G
gnomAD v3:
7-33273080-A-G
gnomAD v4:
7-33273080-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.33273080A>G , CM000669.2:g.33273080A>G | GRCh38 |
| NC_000007.13:g.33312692A>G , CM000669.1:g.33312692A>G | GRCh37 |
| NC_000007.12:g.33279217A>G | NCBI36 |
| NG_009306.1:g.148541A>G | |
| NG_009306.2:g.148837A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242067.11:c.771A>G MANE Select | ENSP00000242067.6:p.Ala257= | |
| ENST00000671871.1:c.894A>G | ENSP00000499908.1:p.Ala298= | |
| ENST00000671890.1:c.636A>G | ENSP00000500146.1:p.Ala212= | |
| ENST00000671952.1:c.771A>G | ENSP00000500239.1:p.Ala257= | |
| ENST00000671963.1:c.405A>G | ENSP00000499904.1:p.Ala135= | |
| ENST00000672453.1:n.540A>G | ||
| ENST00000672717.1:c.771A>G | ENSP00000499835.1:p.Ala257= | |
| ENST00000672973.1:c.771A>G | ENSP00000500017.1:p.Ala257= | |
| ENST00000673056.1:c.771A>G | ENSP00000499989.1:p.Ala257= | |
| ENST00000673219.1:c.*508A>G | ENSP00000499968.1:n.*508A>G | |
| ENST00000673230.1:n.802A>G | ||
| ENST00000673431.1:c.636A>G | ENSP00000500552.1:p.Ala212= | |
| ENST00000673462.1:c.771A>G | ENSP00000499848.1:p.Ala257= | |
| ENST00000242067.10:c.771A>G | ENSP00000242067.6:p.Ala257= | |
| ENST00000350941.7:c.771A>G | ENSP00000313122.6:p.Ala257= | |
| ENST00000355070.6:c.771A>G | ENSP00000347182.2:p.Ala257= | |
| ENST00000396127.6:c.771A>G | ENSP00000379433.2:p.Ala257= | |
| ENST00000425508.6:c.636A>G | ENSP00000405151.2:p.Ala212= | |
| ENST00000433714.5:c.771A>G | ENSP00000412159.1:p.Ala257= | |
| ENST00000442858.1:c.405A>G | ENSP00000388646.1:p.Ala135= | |
| NM_001033604.1:c.771A>G | NP_001028776.1:p.Ala257= | |
| NM_001033605.1:c.771A>G | NP_001028777.1:p.Ala257= | |
| NM_014451.3:c.771A>G | NP_055266.2:p.Ala257= | |
| NM_198428.2:c.771A>G | NP_940820.1:p.Ala257= | |
| XM_005249700.3:c.771A>G | XP_005249757.1:p.Ala257= | |
| XM_005249701.1:c.771A>G | XP_005249758.1:p.Ala257= | |
| XM_011515264.1:c.771A>G | XP_011513566.1:p.Ala257= | |
| XM_011515265.1:c.771A>G | XP_011513567.1:p.Ala257= | |
| XM_011515266.1:c.771A>G | XP_011513568.1:p.Ala257= | |
| XM_011515267.1:c.771A>G | XP_011513569.1:p.Ala257= | |
| XM_011515268.1:c.771A>G | XP_011513570.1:p.Ala257= | |
| XM_011515269.1:c.498A>G | XP_011513571.1:p.Ala166= | |
| XM_011515270.1:c.771A>G | XP_011513572.1:p.Ala257= | |
| NM_001348036.1:c.771A>G | NP_001334965.1:p.Ala257= | |
| NM_001348037.2:c.405A>G | NP_001334966.1:p.Ala135= | |
| NM_001348038.2:c.498A>G | NP_001334967.1:p.Ala166= | |
| NM_001348039.2:c.498A>G | NP_001334968.1:p.Ala166= | |
| NM_001348040.2:c.771A>G | NP_001334969.1:p.Ala257= | |
| NM_001348041.3:c.771A>G | NP_001334970.1:p.Ala257= | |
| NM_001348042.2:c.636A>G | NP_001334971.1:p.Ala212= | |
| NM_001348043.2:c.771A>G | NP_001334972.1:p.Ala257= | |
| NM_001348044.2:c.405A>G | NP_001334973.1:p.Ala135= | |
| NM_001348045.2:c.405A>G | NP_001334974.1:p.Ala135= | |
| NM_001348046.2:c.405A>G | NP_001334975.1:p.Ala135= | |
| NM_001362679.1:c.771A>G | NP_001349608.1:p.Ala257= | |
| NR_145411.1:n.1050A>G | ||
| NR_145412.1:n.1050A>G | ||
| NR_145413.2:n.1284A>G | ||
| XM_005249701.3:c.771A>G | XP_005249758.1:p.Ala257= | |
| XM_011515265.2:c.771A>G | XP_011513567.1:p.Ala257= | |
| XM_011515266.3:c.771A>G | XP_011513568.1:p.Ala257= | |
| XM_011515267.3:c.771A>G | XP_011513569.1:p.Ala257= | |
| XM_011515269.2:c.498A>G | XP_011513571.1:p.Ala166= | |
| XM_011515270.3:c.771A>G | XP_011513572.1:p.Ala257= | |
| XM_017011990.1:c.771A>G | XP_016867479.1:p.Ala257= | |
| XM_017011994.2:c.771A>G | XP_016867483.1:p.Ala257= | |
| XR_001744634.2:n.1274A>G | ||
| NM_001348040.3:c.771A>G | NP_001334969.1:p.Ala257= | |
| NM_001348041.4:c.771A>G | NP_001334970.1:p.Ala257= | |
| NM_001348043.3:c.771A>G | NP_001334972.1:p.Ala257= | |
| NM_198428.3:c.771A>G MANE Select | NP_940820.1:p.Ala257= | |
| NM_001033604.2:c.771A>G | NP_001028776.1:p.Ala257= | |
| NM_001033605.2:c.771A>G | NP_001028777.1:p.Ala257= | |
| NM_001348037.3:c.405A>G | NP_001334966.1:p.Ala135= | |
| NM_001348038.3:c.498A>G | NP_001334967.1:p.Ala166= | |
| NM_001348039.3:c.498A>G | NP_001334968.1:p.Ala166= | |
| NM_001348042.3:c.636A>G | NP_001334971.1:p.Ala212= | |
| NM_001348044.3:c.405A>G | NP_001334973.1:p.Ala135= | |
| NM_001348045.3:c.405A>G | NP_001334974.1:p.Ala135= | |
| NM_001348046.3:c.405A>G | NP_001334975.1:p.Ala135= | |
| NM_014451.4:c.771A>G | NP_055266.2:p.Ala257= | |
| NR_145413.3:n.1260A>G |