HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547549C>A , CM000680.2:g.31547549C>A | GRCh38 |
NC_000018.9:g.29127512C>A , CM000680.1:g.29127512C>A | GRCh37 |
NC_000018.8:g.27381510C>A | NCBI36 |
NG_007072.3:g.54308C>A , LRG_397:g.54308C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*806C>A (DSG2) MANE Select | ENSP00000261590.8:n.*806C>A | |
ENST00000261590.12:c.*806C>A (DSG2) | ENSP00000261590.8:n.*806C>A | |
NM_001943.3:c.*806C>A , LRG_397t1:c.*806C>A (DSG2) | NP_001934.2:n.*806C>A | |
NR_045216.1:n.1346-1643G>T (DSG2-AS1) | ||
NM_001943.4:c.*806C>A (DSG2) | NP_001934.2:n.*806C>A | |
NM_001943.5:c.*806C>A (DSG2) MANE Select | NP_001934.2:n.*806C>A |