HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547794T= , CM000680.2:g.31547794T= | GRCh38 |
NC_000018.9:g.29127757T= , CM000680.1:g.29127757T= | GRCh37 |
NC_000018.8:g.27381755T= | NCBI36 |
NG_007072.3:g.54553T= , LRG_397:g.54553T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*1051T= (DSG2) MANE Select | ENSP00000261590.8:n.*1051T= | |
ENST00000261590.12:c.*1051T= (DSG2) | ENSP00000261590.8:n.*1051T= | |
NM_001943.3:c.*1051T= , LRG_397t1:c.*1051T= (DSG2) | NP_001934.2:n.*1051T= | |
NR_045216.1:n.1346-1888A= (DSG2-AS1) | ||
NM_001943.4:c.*1051T= (DSG2) | NP_001934.2:n.*1051T= | |
NM_001943.5:c.*1051T= (DSG2) MANE Select | NP_001934.2:n.*1051T= |