Linked Data
ClinVar Variation Id:
92306
dbSNP Id:
rs143977255
ExAC:
22:40756439 A / T
gnomAD v2:
22-40756439-A-T
gnomAD v3:
22-40360435-A-T
gnomAD v4:
22-40360435-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.40360435A>T , CM000684.2:g.40360435A>T | GRCh38 |
| NC_000022.10:g.40756439A>T , CM000684.1:g.40756439A>T | GRCh37 |
| NC_000022.9:g.39086385A>T | NCBI36 |
| NG_007993.1:g.18936A>T | |
| NG_007993.2:g.18936A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480775.3:c.735A>T | ENSP00000485462.2:p.Arg245= | |
| ENST00000623287.4:c.*160A>T | ENSP00000485437.1:n.*160A>T | |
| ENST00000623632.4:c.735A>T | ENSP00000485288.2:p.Arg245= | |
| ENST00000625194.4:c.735A>T | ENSP00000485289.2:p.Arg245= | |
| ENST00000636265.1:c.735A>T | ENSP00000490909.1:p.Arg245= | |
| ENST00000636433.1:n.757A>T | ||
| ENST00000636714.1:c.735A>T | ENSP00000490946.1:p.Arg245= | |
| ENST00000637666.2:c.735A>T | ENSP00000489696.2:p.Arg245= | |
| ENST00000637669.1:c.735A>T | ENSP00000489728.1:p.Arg245= | |
| ENST00000639722.1:c.*431A>T | ENSP00000492828.1:n.*431A>T | |
| ENST00000674592.1:n.759A>T | ||
| ENST00000675622.1:n.3802A>T | ||
| ENST00000679609.1:c.*160A>T | ENSP00000506592.1:n.*160A>T | |
| ENST00000679656.1:n.640A>T | ||
| ENST00000679723.1:c.690A>T | ENSP00000505155.1:p.Arg230= | |
| ENST00000679845.1:n.858A>T | ||
| ENST00000679904.1:n.946A>T | ||
| ENST00000680378.1:c.822A>T | ENSP00000505556.1:p.Arg274= | |
| ENST00000680444.1:c.735A>T | ENSP00000505298.1:p.Arg245= | |
| ENST00000680978.1:c.735A>T | ENSP00000505244.1:p.Arg245= | |
| ENST00000681003.1:n.167A>T | ||
| ENST00000681159.1:n.794A>T | ||
| ENST00000216194.11:c.777A>T | ENSP00000216194.8:p.Arg259= | |
| ENST00000342312.9:c.735A>T | ENSP00000341429.6:p.Arg245= | |
| ENST00000480775.2:c.149A>T | ||
| ENST00000623063.3:c.735A>T MANE Select | ENSP00000485525.1:p.Arg245= | |
| ENST00000623287.3:c.*160A>T | ENSP00000485437.1:n.*160A>T | |
| ENST00000623632.3:c.690A>T | ENSP00000485288.1:p.Arg230= | |
| ENST00000623978.3:c.195A>T | ENSP00000485477.1:p.Arg65= | |
| ENST00000625194.3:c.322A>T | ||
| NM_000026.2:c.735A>T | NP_000017.1:p.Arg245= | |
| NM_001123378.1:c.735A>T | NP_001116850.1:p.Arg245= | |
| XM_011529976.1:c.735A>T | XP_011528278.1:p.Arg245= | |
| XM_011529977.1:c.735A>T | XP_011528279.1:p.Arg245= | |
| XM_011529978.1:c.735A>T | XP_011528280.1:p.Arg245= | |
| XM_011529979.1:c.735A>T | XP_011528281.1:p.Arg245= | |
| XM_011529980.1:c.735A>T | XP_011528282.1:p.Arg245= | |
| XM_011529981.1:c.270A>T | XP_011528283.1:p.Arg90= | |
| XM_011529982.1:c.-282A>T | XP_011528284.1:n.-282A>T | |
| XR_937824.1:n.794A>T | ||
| XR_937825.1:n.794A>T | ||
| XR_937826.1:n.794A>T | ||
| NM_000026.3:c.735A>T | NP_000017.1:p.Arg245= | |
| NM_001123378.2:c.735A>T | NP_001116850.1:p.Arg245= | |
| NM_001317923.1:c.543A>T | NP_001304852.1:p.Arg181= | |
| NM_001363840.1:c.735A>T | NP_001350769.1:p.Arg245= | |
| NR_134256.1:n.794A>T | ||
| XM_011529977.3:c.735A>T | XP_011528279.1:p.Arg245= | |
| XM_011529980.3:c.735A>T | XP_011528282.1:p.Arg245= | |
| XM_017028636.1:c.690A>T | XP_016884125.1:p.Arg230= | |
| XM_017028637.1:c.690A>T | XP_016884126.1:p.Arg230= | |
| XM_017028638.1:c.270A>T | XP_016884127.1:p.Arg90= | |
| XM_017028639.2:c.270A>T | XP_016884128.1:p.Arg90= | |
| XM_017028640.1:c.-282A>T | XP_016884129.1:n.-282A>T | |
| XM_024452166.1:c.690A>T | XP_024307934.1:p.Arg230= | |
| XR_001755176.2:n.792A>T | ||
| XR_002958670.1:n.731A>T | ||
| XR_002958671.1:n.792A>T | ||
| XR_937825.3:n.792A>T | ||
| NM_000026.4:c.735A>T MANE Select | NP_000017.1:p.Arg245= | |
| NM_001363840.2:c.735A>T | NP_001350769.1:p.Arg245= | |
| NM_001123378.3:c.735A>T | NP_001116850.1:p.Arg245= | |
| NM_001317923.2:c.543A>T | NP_001304852.1:p.Arg181= | |
| NM_001363840.3:c.735A>T | NP_001350769.1:p.Arg245= | |
| NR_134256.2:n.794A>T |