Linked Data
ClinVar Variation Id:
222569
ClinVar RCV Id:
RCV000208322
dbSNP Id:
rs528851283
gnomAD v2:
18-29125677-A-G
gnomAD v3:
18-31545714-A-G
gnomAD v4:
18-31545714-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31545714A>G , CM000680.2:g.31545714A>G | GRCh38 |
| NC_000018.9:g.29125677A>G , CM000680.1:g.29125677A>G | GRCh37 |
| NC_000018.8:g.27379675A>G | NCBI36 |
| NG_007072.3:g.52473A>G , LRG_397:g.52473A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261590.13:c.2335-7A>G (DSG2) MANE Select | ENSP00000261590.8:n.2335-7A>G | |
| ENST00000261590.12:c.2335-7A>G (DSG2) | ENSP00000261590.8:n.2335-7A>G | |
| NM_001943.3:c.2335-7A>G , LRG_397t1:c.2335-7A>G (DSG2) | NP_001934.2:n.2335-7A>G | |
| NR_045216.1:n.1516+22T>C (DSG2-AS1) | ||
| NM_001943.4:c.2335-7A>G (DSG2) | NP_001934.2:n.2335-7A>G | |
| XM_024451095.1:c.1801-7A>G (DSG2) | XP_024306863.1:n.1801-7A>G | |
| NM_001943.5:c.2335-7A>G (DSG2) MANE Select | NP_001934.2:n.2335-7A>G |