HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546346T>C , CM000680.2:g.31546346T>C | GRCh38 |
NC_000018.9:g.29126309T>C , CM000680.1:g.29126309T>C | GRCh37 |
NC_000018.8:g.27380307T>C | NCBI36 |
NG_007072.3:g.53105T>C , LRG_397:g.53105T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.2960T>C (DSG2) MANE Select | ENSP00000261590.8:p.Val987Ala | |
ENST00000261590.12:c.2960T>C (DSG2) | ENSP00000261590.8:p.Val987Ala | |
NM_001943.3:c.2960T>C , LRG_397t1:c.2960T>C (DSG2) | NP_001934.2:p.Val987Ala | |
NR_045216.1:n.1346-440A>G (DSG2-AS1) | ||
NM_001943.4:c.2960T>C (DSG2) | NP_001934.2:p.Val987Ala | |
XM_024451095.1:c.2426T>C (DSG2) | XP_024306863.1:p.Val809Ala | |
NM_001943.5:c.2960T>C (DSG2) MANE Select | NP_001934.2:p.Val987Ala |