HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547550G>A , CM000680.2:g.31547550G>A | GRCh38 |
NC_000018.9:g.29127513G>A , CM000680.1:g.29127513G>A | GRCh37 |
NC_000018.8:g.27381511G>A | NCBI36 |
NG_007072.3:g.54309G>A , LRG_397:g.54309G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*807G>A (DSG2) MANE Select | ENSP00000261590.8:n.*807G>A | |
ENST00000261590.12:c.*807G>A (DSG2) | ENSP00000261590.8:n.*807G>A | |
NM_001943.3:c.*807G>A , LRG_397t1:c.*807G>A (DSG2) | NP_001934.2:n.*807G>A | |
NR_045216.1:n.1346-1644C>T (DSG2-AS1) | ||
NM_001943.4:c.*807G>A (DSG2) | NP_001934.2:n.*807G>A | |
NM_001943.5:c.*807G>A (DSG2) MANE Select | NP_001934.2:n.*807G>A |