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MyVariant.info:
GRCh37
chr18:g.29126598C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31546635C>T , CM000680.2:g.31546635C>T | GRCh38 |
| NC_000018.9:g.29126598C>T , CM000680.1:g.29126598C>T | GRCh37 |
| NC_000018.8:g.27380596C>T | NCBI36 |
| NG_007072.3:g.53394C>T , LRG_397:g.53394C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.3249C>T (DSG2) MANE Select | ENSP00000261590.8:p.Gly1083= | |
| ENST00000261590.12:c.3249C>T (DSG2) | ENSP00000261590.8:p.Gly1083= | |
| NM_001943.3:c.3249C>T , LRG_397t1:c.3249C>T (DSG2) | NP_001934.2:p.Gly1083= | |
| NR_045216.1:n.1346-729G>A (DSG2-AS1) | ||
| NM_001943.4:c.3249C>T (DSG2) | NP_001934.2:p.Gly1083= | |
| XM_024451095.1:c.2715C>T (DSG2) | XP_024306863.1:p.Gly905= | |
| NM_001943.5:c.3249C>T (DSG2) MANE Select | NP_001934.2:p.Gly1083= |