Linked Data
MyVariant Identifiers:
chr18:g.29126245A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31546282A>C , CM000680.2:g.31546282A>C | GRCh38 |
| NC_000018.9:g.29126245A>C , CM000680.1:g.29126245A>C | GRCh37 |
| NC_000018.8:g.27380243A>C | NCBI36 |
| NG_007072.3:g.53041A>C , LRG_397:g.53041A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.2896A>C (DSG2) MANE Select | ENSP00000261590.8:p.Arg966= | |
| ENST00000261590.12:c.2896A>C (DSG2) | ENSP00000261590.8:p.Arg966= | |
| NM_001943.3:c.2896A>C , LRG_397t1:c.2896A>C (DSG2) | NP_001934.2:p.Arg966= | |
| NR_045216.1:n.1346-376T>G (DSG2-AS1) | ||
| NM_001943.4:c.2896A>C (DSG2) | NP_001934.2:p.Arg966= | |
| XM_024451095.1:c.2362A>C (DSG2) | XP_024306863.1:p.Arg788= | |
| NM_001943.5:c.2896A>C (DSG2) MANE Select | NP_001934.2:p.Arg966= |