HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31542654C>G , CM000680.2:g.31542654C>G | GRCh38 |
NC_000018.9:g.29122617C>G , CM000680.1:g.29122617C>G | GRCh37 |
NC_000018.8:g.27376615C>G | NCBI36 |
NG_007072.3:g.49413C>G , LRG_397:g.49413C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.2136C>G (DSG2) MANE Select | ENSP00000261590.8:p.Ser712= | |
ENST00000261590.12:c.2136C>G (DSG2) | ENSP00000261590.8:p.Ser712= | |
NM_001943.3:c.2136C>G , LRG_397t1:c.2136C>G (DSG2) | NP_001934.2:p.Ser712= | |
NR_045216.1:n.1811-333G>C (DSG2-AS1) | ||
NM_001943.4:c.2136C>G (DSG2) | NP_001934.2:p.Ser712= | |
XM_024451095.1:c.1602C>G (DSG2) | XP_024306863.1:p.Ser534= | |
NM_001943.5:c.2136C>G (DSG2) MANE Select | NP_001934.2:p.Ser712= |