Linked Data
ClinVar Variation Id:
2075432
ClinVar RCV Id:
RCV002967721
dbSNP Id:
rs370415753
ExAC:
12:48535549 A / G
gnomAD v2:
12-48535549-A-G
gnomAD v3:
12-48141766-A-G
gnomAD v4:
12-48141766-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48141766A>G , CM000674.2:g.48141766A>G | GRCh38 |
| NC_000012.11:g.48535549A>G , CM000674.1:g.48535549A>G | GRCh37 |
| NC_000012.10:g.46821816A>G | NCBI36 |
| NG_016199.1:g.40894A>G | |
| NG_016199.2:g.41514A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000550257.7:c.1661A>G | ENSP00000447997.3:p.Gln554Arg | |
| ENST00000340802.12:c.1652A>G | ENSP00000345771.6:p.Gln551Arg | |
| ENST00000359794.11:c.1439A>G MANE Select | ENSP00000352842.5:p.Gln480Arg | |
| ENST00000549941.7:c.1346A>G | ENSP00000446829.3:p.Gln449Arg | |
| ENST00000550345.6:c.1439A>G | ENSP00000450369.2:p.Gln480Arg | |
| ENST00000550924.6:c.1439A>G | ENSP00000446945.2:p.Gln480Arg | |
| ENST00000551339.6:c.1439A>G | ENSP00000448253.2:p.Gln480Arg | |
| ENST00000642730.1:c.1748A>G | ENSP00000496597.1:p.Gln583Arg | |
| ENST00000312352.11:c.1439A>G | ENSP00000309438.7:p.Gln480Arg | |
| ENST00000340802.10:c.1652A>G | ENSP00000345771.6:p.Gln551Arg | |
| ENST00000359794.9:c.1439A>G | ENSP00000352842.5:p.Gln480Arg | |
| ENST00000546465.1:c.284A>G | ENSP00000446519.1:p.Gln95Arg | |
| ENST00000546964.5:n.1763A>G | ||
| ENST00000547581.5:c.*1707A>G | ENSP00000447992.1:n.*1707A>G | |
| ENST00000547587.5:c.1439A>G | ENSP00000449426.1:p.Gln480Arg | |
| ENST00000550802.1:n.71A>G | ||
| ENST00000551804.5:c.1346A>G | ENSP00000448177.1:p.Gln449Arg | |
| ENST00000552214.1:n.95A>G | ||
| ENST00000552752.5:c.588A>G | ||
| ENST00000552818.1:n.62A>G | ||
| NM_000289.5:c.1439A>G | NP_000280.1:p.Gln480Arg | |
| NM_001166686.1:c.1652A>G | NP_001160158.1:p.Gln551Arg | |
| NM_001166687.1:c.1439A>G | NP_001160159.1:p.Gln480Arg | |
| NM_001166688.1:c.1439A>G | NP_001160160.1:p.Gln480Arg | |
| XM_005268974.1:c.1748A>G | XP_005269031.1:p.Gln583Arg | |
| XM_005268975.1:c.1748A>G | XP_005269032.1:p.Gln583Arg | |
| XM_005268976.2:c.1748A>G | XP_005269033.1:p.Gln583Arg | |
| XM_005268977.1:c.1652A>G | XP_005269034.1:p.Gln551Arg | |
| XM_005268978.2:c.1652A>G | XP_005269035.1:p.Gln551Arg | |
| XM_005268979.1:c.1652A>G | XP_005269036.1:p.Gln551Arg | |
| XM_011538487.1:c.1655A>G | XP_011536789.1:p.Gln552Arg | |
| XM_011538488.1:c.1439A>G | XP_011536790.1:p.Gln480Arg | |
| NM_000289.6:c.1439A>G MANE Select | NP_000280.1:p.Gln480Arg | |
| NM_001166686.2:c.1652A>G | NP_001160158.1:p.Gln551Arg | |
| NM_001354735.1:c.1748A>G | NP_001341664.1:p.Gln583Arg | |
| NM_001354736.1:c.1748A>G | NP_001341665.1:p.Gln583Arg | |
| NM_001354737.1:c.1652A>G | NP_001341666.1:p.Gln551Arg | |
| NM_001354738.1:c.1652A>G | NP_001341667.1:p.Gln551Arg | |
| NM_001354739.1:c.1652A>G | NP_001341668.1:p.Gln551Arg | |
| NM_001354740.1:c.1583A>G | NP_001341669.1:p.Gln528Arg | |
| NM_001354741.1:c.1463A>G | NP_001341670.1:p.Gln488Arg | |
| NM_001354742.1:c.1439A>G | NP_001341671.1:p.Gln480Arg | |
| NM_001354743.1:c.1439A>G | NP_001341672.1:p.Gln480Arg | |
| NM_001354744.1:c.1439A>G | NP_001341673.1:p.Gln480Arg | |
| NM_001354745.1:c.1352A>G | NP_001341674.1:p.Gln451Arg | |
| NM_001354746.1:c.1313A>G | NP_001341675.1:p.Gln438Arg | |
| NM_001354747.1:c.1289A>G | NP_001341676.1:p.Gln430Arg | |
| NM_001354748.1:c.1289A>G | NP_001341677.1:p.Gln430Arg | |
| NM_001363619.1:c.1346A>G | NP_001350548.1:p.Gln449Arg | |
| NR_148954.1:n.1876A>G | ||
| NR_148955.1:n.2512A>G | ||
| NR_148956.1:n.1802A>G | ||
| NR_148957.1:n.2031A>G | ||
| NR_148958.1:n.1779A>G | ||
| NR_148959.1:n.1705A>G | ||
| XM_005268976.3:c.1748A>G | XP_005269033.1:p.Gln583Arg | |
| XM_017019469.1:c.1559A>G | XP_016874958.1:p.Gln520Arg | |
| XM_024449020.1:c.1661A>G | XP_024304788.1:p.Gln554Arg | |
| XM_024449021.1:c.1538A>G | XP_024304789.1:p.Gln513Arg | |
| XM_024449022.1:c.1439A>G | XP_024304790.1:p.Gln480Arg | |
| NM_001166687.2:c.1439A>G | NP_001160159.1:p.Gln480Arg | |
| NM_001166688.2:c.1439A>G | NP_001160160.1:p.Gln480Arg | |
| NM_001354741.2:c.1463A>G | NP_001341670.1:p.Gln488Arg | |
| NM_001354742.2:c.1439A>G | NP_001341671.1:p.Gln480Arg | |
| NM_001354743.2:c.1439A>G | NP_001341672.1:p.Gln480Arg | |
| NM_001354744.2:c.1439A>G | NP_001341673.1:p.Gln480Arg | |
| NM_001354745.2:c.1352A>G | NP_001341674.1:p.Gln451Arg | |
| NM_001354746.2:c.1313A>G | NP_001341675.1:p.Gln438Arg | |
| NM_001354747.2:c.1289A>G | NP_001341676.1:p.Gln430Arg | |
| NM_001354748.2:c.1289A>G | NP_001341677.1:p.Gln430Arg | |
| NM_001363619.2:c.1346A>G | NP_001350548.1:p.Gln449Arg | |
| NR_148954.2:n.1742A>G | ||
| NR_148956.2:n.1668A>G | ||
| NR_148957.2:n.1897A>G | ||
| NR_148958.2:n.1645A>G | ||
| NR_148959.2:n.1571A>G |