HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48037719C= , CM000675.2:g.48037719C= | GRCh38 |
NC_000013.10:g.48611855C= , CM000675.1:g.48611855C= | GRCh37 |
NC_000013.9:g.47509856C= | NCBI36 |
NG_047021.1:g.5153C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643246.1:c.-276G= (SUCLA2) | ENSP00000496235.1:n.-276G= | |
ENST00000646804.1:c.-198G= (SUCLA2) | ENSP00000493977.1:n.-198G= | |
ENST00000258662.2:c.-28C= (NUDT15) | ENSP00000258662.1:n.-28C= | |
NM_001304745.1:c.-28C= (NUDT15) | NP_001291674.1:n.-28C= | |
NM_018283.2:c.-28C= (NUDT15) | NP_060753.1:n.-28C= | |
NM_018283.3:c.-28C= (NUDT15) | NP_060753.1:n.-28C= | |
NR_136687.1:n.153C= (NUDT15) | ||
NR_136688.1:n.153C= (NUDT15) |