Linked Data
dbSNP Id:
rs767996100
ExAC:
1:67724506 A / G
gnomAD v2:
1-67724506-A-G
gnomAD v4:
1-67258823-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67258823A>G , CM000663.2:g.67258823A>G | GRCh38 |
| NC_000001.10:g.67724506A>G , CM000663.1:g.67724506A>G | GRCh37 |
| NC_000001.9:g.67497094A>G | NCBI36 |
| NG_011498.1:g.97338A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697149.1:c.1424A>G | ENSP00000513138.1:n.1424A>G | |
| ENST00000697150.1:c.1482A>G | ENSP00000513139.1:n.1482A>G | |
| ENST00000697151.1:c.1415A>G | ENSP00000513140.1:n.1415A>G | |
| ENST00000697164.1:c.1495A>G | ENSP00000513153.1:p.Asn499Asp | |
| ENST00000697165.1:c.1282A>G | ENSP00000513154.1:p.Asn428Asp | |
| ENST00000347310.10:c.1585A>G MANE Select | ENSP00000321345.5:p.Asn529Asp | |
| ENST00000637002.1:c.976A>G | ENSP00000490340.1:p.Asn326Asp | |
| ENST00000347310.9:c.1585A>G | ENSP00000321345.5:p.Asn529Asp | |
| ENST00000395227.2:c.379A>G | ENSP00000378652.2:p.Asn127Asp | |
| ENST00000425614.3:c.820A>G | ENSP00000387640.2:p.Asn274Asp | |
| ENST00000473881.2:c.*411A>G | ENSP00000486667.1:n.*411A>G | |
| NM_144701.2:c.1585A>G | NP_653302.2:p.Asn529Asp | |
| XM_005270516.2:c.823A>G | XP_005270573.1:p.Asn275Asp | |
| XM_011540789.1:c.1675A>G | XP_011539091.1:p.Asn559Asp | |
| XM_011540790.1:c.1585A>G | XP_011539092.1:p.Asn529Asp | |
| XM_011540791.1:c.1585A>G | XP_011539093.1:p.Asn529Asp | |
| XM_011540790.3:c.1585A>G | XP_011539092.1:p.Asn529Asp | |
| XM_011540791.3:c.1585A>G | XP_011539093.1:p.Asn529Asp | |
| XR_001736993.1:n.1665A>G | ||
| NM_144701.3:c.1585A>G MANE Select | NP_653302.2:p.Asn529Asp |