Linked Data
ClinVar Variation Id:
517918
dbSNP Id:
rs774775322
ExAC:
18:29125932 A / G
gnomAD v2:
18-29125932-A-G
gnomAD v3:
18-31545969-A-G
gnomAD v4:
18-31545969-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31545969A>G , CM000680.2:g.31545969A>G | GRCh38 |
| NC_000018.9:g.29125932A>G , CM000680.1:g.29125932A>G | GRCh37 |
| NC_000018.8:g.27379930A>G | NCBI36 |
| NG_007072.3:g.52728A>G , LRG_397:g.52728A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261590.13:c.2583A>G (DSG2) MANE Select | ENSP00000261590.8:p.Thr861= | |
| ENST00000261590.12:c.2583A>G (DSG2) | ENSP00000261590.8:p.Thr861= | |
| NM_001943.3:c.2583A>G , LRG_397t1:c.2583A>G (DSG2) | NP_001934.2:p.Thr861= | |
| NR_045216.1:n.1346-63T>C (DSG2-AS1) | ||
| NM_001943.4:c.2583A>G (DSG2) | NP_001934.2:p.Thr861= | |
| XM_024451095.1:c.2049A>G (DSG2) | XP_024306863.1:p.Thr683= | |
| NM_001943.5:c.2583A>G (DSG2) MANE Select | NP_001934.2:p.Thr861= |