HGVS | Genome Assembly |
---|---|
NC_000005.10:g.119452481T>C , CM000667.2:g.119452481T>C | GRCh38 |
NC_000005.9:g.118788176T>C , CM000667.1:g.118788176T>C | GRCh37 |
NC_000005.8:g.118816075T>C | NCBI36 |
NG_008182.1:g.5029T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000509514.6:c.-95T>C | ENSP00000426272.2:n.-95T>C | |
ENST00000682996.1:c.-95T>C | ENSP00000507792.1:n.-95T>C | |
ENST00000683936.1:c.-95T>C | ENSP00000507721.1:n.-95T>C | |
ENST00000684214.1:c.-95T>C | ENSP00000508071.1:n.-95T>C | |
ENST00000256216.10:c.-95T>C | ENSP00000256216.6:n.-95T>C | |
ENST00000511186.5:n.9T>C | ||
NM_000414.3:c.-95T>C | NP_000405.1:n.-95T>C | |
NM_001199292.1:c.-95T>C | NP_001186221.1:n.-95T>C | |
NM_001292027.1:c.-232T>C | NP_001278956.1:n.-232T>C |