HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546463G>A , CM000680.2:g.31546463G>A | GRCh38 |
NC_000018.9:g.29126426G>A , CM000680.1:g.29126426G>A | GRCh37 |
NC_000018.8:g.27380424G>A | NCBI36 |
NG_007072.3:g.53222G>A , LRG_397:g.53222G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.3077G>A (DSG2) MANE Select | ENSP00000261590.8:p.Ser1026Asn | |
ENST00000261590.12:c.3077G>A (DSG2) | ENSP00000261590.8:p.Ser1026Asn | |
NM_001943.3:c.3077G>A , LRG_397t1:c.3077G>A (DSG2) | NP_001934.2:p.Ser1026Asn | |
NR_045216.1:n.1346-557C>T (DSG2-AS1) | ||
NM_001943.4:c.3077G>A (DSG2) | NP_001934.2:p.Ser1026Asn | |
XM_024451095.1:c.2543G>A (DSG2) | XP_024306863.1:p.Ser848Asn | |
NM_001943.5:c.3077G>A (DSG2) MANE Select | NP_001934.2:p.Ser1026Asn |