Linked Data
MyVariant Identifiers:
chr18:g.29126115A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31546152A>T , CM000680.2:g.31546152A>T | GRCh38 |
| NC_000018.9:g.29126115A>T , CM000680.1:g.29126115A>T | GRCh37 |
| NC_000018.8:g.27380113A>T | NCBI36 |
| NG_007072.3:g.52911A>T , LRG_397:g.52911A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.2766A>T (DSG2) MANE Select | ENSP00000261590.8:p.Thr922= | |
| ENST00000261590.12:c.2766A>T (DSG2) | ENSP00000261590.8:p.Thr922= | |
| NM_001943.3:c.2766A>T , LRG_397t1:c.2766A>T (DSG2) | NP_001934.2:p.Thr922= | |
| NR_045216.1:n.1346-246T>A (DSG2-AS1) | ||
| NM_001943.4:c.2766A>T (DSG2) | NP_001934.2:p.Thr922= | |
| XM_024451095.1:c.2232A>T (DSG2) | XP_024306863.1:p.Thr744= | |
| NM_001943.5:c.2766A>T (DSG2) MANE Select | NP_001934.2:p.Thr922= |