Linked Data
ClinVar Variation Id:
349383
dbSNP Id:
rs768939011
ExAC:
4:657583 A / G
gnomAD v2:
4-657583-A-G
gnomAD v3:
4-663794-A-G
gnomAD v4:
4-663794-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.663794A>G , CM000666.2:g.663794A>G | GRCh38 |
| NC_000004.11:g.657583A>G , CM000666.1:g.657583A>G | GRCh37 |
| NC_000004.10:g.647583A>G | NCBI36 |
| NG_009839.1:g.43221A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496514.6:c.1945A>G MANE Select | ENSP00000420295.1:p.Asn649Asp | |
| ENST00000255622.10:c.1945A>G | ENSP00000255622.6:p.Asn649Asp | |
| ENST00000429163.6:c.1108A>G | ENSP00000406334.2:p.Asn370Asp | |
| ENST00000460119.1:n.72A>G | ||
| ENST00000471824.6:c.25A>G | ENSP00000417852.2:p.Asn9Asp | |
| ENST00000496514.5:c.1945A>G | ENSP00000420295.1:p.Asn649Asp | |
| NM_000283.3:c.1945A>G | NP_000274.2:p.Asn649Asp | |
| NM_001145291.1:c.1945A>G | NP_001138763.1:p.Asn649Asp | |
| NM_001145292.1:c.1108A>G | NP_001138764.1:p.Asn370Asp | |
| XM_011513473.1:c.2164A>G | XP_011511775.1:p.Asn722Asp | |
| XM_011513474.1:c.2164A>G | XP_011511776.1:p.Asn722Asp | |
| XM_011513475.1:c.1945A>G | XP_011511777.1:p.Asn649Asp | |
| XM_011513476.1:c.2164A>G | XP_011511778.1:p.Asn722Asp | |
| XM_011513477.1:c.1150A>G | XP_011511779.1:p.Asn384Asp | |
| XM_011513478.1:c.874A>G | XP_011511780.1:p.Asn292Asp | |
| XR_925029.1:n.87+292T>C | ||
| NM_001350154.1:c.1108A>G | NP_001337083.1:p.Asn370Asp | |
| NM_001350155.1:c.790A>G | NP_001337084.1:p.Asn264Asp | |
| XM_011513473.3:c.2164A>G | XP_011511775.1:p.Asn722Asp | |
| XM_011513474.3:c.2164A>G | XP_011511776.1:p.Asn722Asp | |
| XM_011513475.2:c.1945A>G | XP_011511777.1:p.Asn649Asp | |
| XM_011513476.3:c.2164A>G | XP_011511778.1:p.Asn722Asp | |
| XM_011513478.2:c.874A>G | XP_011511780.1:p.Asn292Asp | |
| XM_017008284.1:c.1108A>G | XP_016863773.1:p.Asn370Asp | |
| XM_017008285.1:c.1108A>G | XP_016863774.1:p.Asn370Asp | |
| XM_017008286.1:c.1108A>G | XP_016863775.1:p.Asn370Asp | |
| NM_001350154.2:c.1108A>G | NP_001337083.1:p.Asn370Asp | |
| NM_001350155.2:c.790A>G | NP_001337084.1:p.Asn264Asp | |
| NM_000283.4:c.1945A>G MANE Select | NP_000274.3:p.Asn649Asp | |
| NM_001145291.2:c.1945A>G | NP_001138763.2:p.Asn649Asp | |
| NM_001145292.2:c.1108A>G | NP_001138764.2:p.Asn370Asp | |
| NM_001350154.3:c.1108A>G | NP_001337083.1:p.Asn370Asp | |
| NM_001350155.3:c.790A>G | NP_001337084.1:p.Asn264Asp | |
| NM_001379246.1:c.1108A>G | NP_001366175.1:p.Asn370Asp | |
| NM_001379247.1:c.1108A>G | NP_001366176.1:p.Asn370Asp |