Linked Data
ClinVar Variation Id:
3002688
ClinVar RCV Id:
RCV003860279
dbSNP Id:
rs768272736
ExAC:
1:67724663 G / C
gnomAD v2:
1-67724663-G-C
gnomAD v3:
1-67258980-G-C
gnomAD v4:
1-67258980-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67258980G>C , CM000663.2:g.67258980G>C | GRCh38 |
| NC_000001.10:g.67724663G>C , CM000663.1:g.67724663G>C | GRCh37 |
| NC_000001.9:g.67497251G>C | NCBI36 |
| NG_011498.1:g.97495G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697149.1:c.1581G>C | ENSP00000513138.1:n.1581G>C | |
| ENST00000697150.1:c.1639G>C | ENSP00000513139.1:n.1639G>C | |
| ENST00000697151.1:c.1572G>C | ENSP00000513140.1:n.1572G>C | |
| ENST00000697164.1:c.1652G>C | ENSP00000513153.1:p.Ser551Thr | |
| ENST00000697165.1:c.1439G>C | ENSP00000513154.1:p.Ser480Thr | |
| ENST00000347310.10:c.1742G>C MANE Select | ENSP00000321345.5:p.Ser581Thr | |
| ENST00000637002.1:c.1133G>C | ENSP00000490340.1:p.Ser378Thr | |
| ENST00000347310.9:c.1742G>C | ENSP00000321345.5:p.Ser581Thr | |
| ENST00000395227.2:c.536G>C | ENSP00000378652.2:p.Ser179Thr | |
| ENST00000425614.3:c.977G>C | ENSP00000387640.2:p.Ser326Thr | |
| ENST00000473881.2:c.*568G>C | ENSP00000486667.1:n.*568G>C | |
| NM_144701.2:c.1742G>C | NP_653302.2:p.Ser581Thr | |
| XM_005270516.2:c.980G>C | XP_005270573.1:p.Ser327Thr | |
| XM_011540789.1:c.1832G>C | XP_011539091.1:p.Ser611Thr | |
| XM_011540790.1:c.1742G>C | XP_011539092.1:p.Ser581Thr | |
| XM_011540791.1:c.1742G>C | XP_011539093.1:p.Ser581Thr | |
| XM_011540790.3:c.1742G>C | XP_011539092.1:p.Ser581Thr | |
| XM_011540791.3:c.1742G>C | XP_011539093.1:p.Ser581Thr | |
| XR_001736993.1:n.1822G>C | ||
| NM_144701.3:c.1742G>C MANE Select | NP_653302.2:p.Ser581Thr |