HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547444A>G , CM000680.2:g.31547444A>G | GRCh38 |
NC_000018.9:g.29127407A>G , CM000680.1:g.29127407A>G | GRCh37 |
NC_000018.8:g.27381405A>G | NCBI36 |
NG_007072.3:g.54203A>G , LRG_397:g.54203A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*701A>G (DSG2) MANE Select | ENSP00000261590.8:n.*701A>G | |
ENST00000261590.12:c.*701A>G (DSG2) | ENSP00000261590.8:n.*701A>G | |
NM_001943.3:c.*701A>G , LRG_397t1:c.*701A>G (DSG2) | NP_001934.2:n.*701A>G | |
NR_045216.1:n.1346-1538T>C (DSG2-AS1) | ||
NM_001943.4:c.*701A>G (DSG2) | NP_001934.2:n.*701A>G | |
XM_024451095.1:c.*701A>G (DSG2) | XP_024306863.1:n.*701A>G | |
NM_001943.5:c.*701A>G (DSG2) MANE Select | NP_001934.2:n.*701A>G |