HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546399A>G , CM000680.2:g.31546399A>G | GRCh38 |
NC_000018.9:g.29126362A>G , CM000680.1:g.29126362A>G | GRCh37 |
NC_000018.8:g.27380360A>G | NCBI36 |
NG_007072.3:g.53158A>G , LRG_397:g.53158A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.3013A>G (DSG2) MANE Select | ENSP00000261590.8:p.Thr1005Ala | |
ENST00000261590.12:c.3013A>G (DSG2) | ENSP00000261590.8:p.Thr1005Ala | |
NM_001943.3:c.3013A>G , LRG_397t1:c.3013A>G (DSG2) | NP_001934.2:p.Thr1005Ala | |
NR_045216.1:n.1346-493T>C (DSG2-AS1) | ||
NM_001943.4:c.3013A>G (DSG2) | NP_001934.2:p.Thr1005Ala | |
XM_024451095.1:c.2479A>G (DSG2) | XP_024306863.1:p.Thr827Ala | |
NM_001943.5:c.3013A>G (DSG2) MANE Select | NP_001934.2:p.Thr1005Ala |