HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547538G= , CM000680.2:g.31547538G= | GRCh38 |
NC_000018.9:g.29127501G= , CM000680.1:g.29127501G= | GRCh37 |
NC_000018.8:g.27381499G= | NCBI36 |
NG_007072.3:g.54297G= , LRG_397:g.54297G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*795G= (DSG2) MANE Select | ENSP00000261590.8:n.*795G= | |
ENST00000261590.12:c.*795G= (DSG2) | ENSP00000261590.8:n.*795G= | |
NM_001943.3:c.*795G= , LRG_397t1:c.*795G= (DSG2) | NP_001934.2:n.*795G= | |
NR_045216.1:n.1346-1632C= (DSG2-AS1) | ||
NM_001943.4:c.*795G= (DSG2) | NP_001934.2:n.*795G= | |
NM_001943.5:c.*795G= (DSG2) MANE Select | NP_001934.2:n.*795G= |