Linked Data
ClinVar Variation Id:
2137879
ClinVar RCV Id:
RCV003041266
dbSNP Id:
rs868921502
gnomAD v2:
X-149809854-G-A
gnomAD v3:
X-150641381-G-A
gnomAD v4:
X-150641381-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.150641381G>A , CM000685.2:g.150641381G>A | GRCh38 |
| NC_000023.10:g.149809854G>A , CM000685.1:g.149809854G>A | GRCh37 |
| NC_000023.9:g.149560512G>A | NCBI36 |
| NG_008199.1:g.77808G>A , LRG_839:g.77808G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684910.1:c.*174G>A | ENSP00000509844.1:n.*174G>A | |
| ENST00000685439.1:c.296G>A | ENSP00000508454.1:p.Arg99Gln | |
| ENST00000685944.1:c.641G>A | ENSP00000509266.1:p.Arg214Gln | |
| ENST00000686212.1:n.243G>A | ||
| ENST00000687215.1:c.*396G>A | ENSP00000509706.1:n.*396G>A | |
| ENST00000688152.1:c.*85G>A | ENSP00000509360.1:n.*85G>A | |
| ENST00000688403.1:c.-104G>A | ENSP00000508944.1:n.-104G>A | |
| ENST00000689314.1:c.686G>A | ENSP00000510607.1:p.Arg229Gln | |
| ENST00000689694.1:c.641G>A | ENSP00000508718.1:p.Arg214Gln | |
| ENST00000689810.1:c.*290G>A | ENSP00000510635.1:n.*290G>A | |
| ENST00000690282.1:c.-104G>A | ENSP00000509809.1:n.-104G>A | |
| ENST00000690351.1:c.*293G>A | ENSP00000509728.1:n.*293G>A | |
| ENST00000691232.1:c.296G>A | ENSP00000509675.1:p.Arg99Gln | |
| ENST00000691482.1:n.1656G>A | ||
| ENST00000691686.1:c.641G>A | ENSP00000509784.1:p.Arg214Gln | |
| ENST00000691851.1:c.641G>A | ENSP00000510106.1:p.Arg214Gln | |
| ENST00000692015.1:c.428G>A | ENSP00000510634.1:p.Arg143Gln | |
| ENST00000692638.1:c.*446G>A | ENSP00000509412.1:n.*446G>A | |
| ENST00000692852.1:c.641G>A | ENSP00000510337.1:p.Arg214Gln | |
| ENST00000692915.1:c.*848G>A | ENSP00000508547.1:n.*848G>A | |
| ENST00000370396.7:c.641G>A MANE Select | ENSP00000359423.3:p.Arg214Gln | |
| ENST00000306167.11:n.508G>A | ||
| ENST00000370396.6:c.641G>A | ENSP00000359423.2:p.Arg214Gln | |
| ENST00000490530.1:n.580G>A | ||
| NM_000252.2:c.641G>A , LRG_839t1:c.641G>A | NP_000243.1:p.Arg214Gln | |
| XM_005274687.2:c.641G>A | XP_005274744.1:p.Arg214Gln | |
| XM_011531170.1:c.707G>A | XP_011529472.1:p.Arg236Gln | |
| XM_011531171.1:c.686G>A | XP_011529473.1:p.Arg229Gln | |
| XM_011531172.1:c.686G>A | XP_011529474.1:p.Arg229Gln | |
| XM_011531173.1:c.641G>A | XP_011529475.1:p.Arg214Gln | |
| XM_011531173.2:c.641G>A | XP_011529475.1:p.Arg214Gln | |
| XM_017029547.1:c.686G>A | XP_016885036.1:p.Arg229Gln | |
| XM_017029548.1:c.686G>A | XP_016885037.1:p.Arg229Gln | |
| XM_017029549.1:c.641G>A | XP_016885038.1:p.Arg214Gln | |
| XM_017029550.1:c.530G>A | XP_016885039.1:p.Arg177Gln | |
| XM_017029551.2:c.-104G>A | XP_016885040.1:n.-104G>A | |
| NM_000252.3:c.641G>A MANE Select | NP_000243.1:p.Arg214Gln | |
| NM_001376906.1:c.641G>A | NP_001363835.1:p.Arg214Gln | |
| NM_001376907.1:c.530G>A | NP_001363836.1:p.Arg177Gln | |
| NM_001376908.1:c.641G>A | NP_001363837.1:p.Arg214Gln |