HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48037595G>T , CM000675.2:g.48037595G>T | GRCh38 |
NC_000013.10:g.48611731G>T , CM000675.1:g.48611731G>T | GRCh37 |
NC_000013.9:g.47509732G>T | NCBI36 |
NG_047021.1:g.5029G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000643246.1:c.-163+11C>A (SUCLA2) | ENSP00000496235.1:n.-163+11C>A | |
ENST00000646804.1:c.-85+11C>A (SUCLA2) | ENSP00000493977.1:n.-85+11C>A | |
ENST00000258662.2:c.-152G>T (NUDT15) | ENSP00000258662.1:n.-152G>T | |
NM_001304745.1:c.-152G>T (NUDT15) | NP_001291674.1:n.-152G>T | |
NM_018283.2:c.-152G>T (NUDT15) | NP_060753.1:n.-152G>T | |
NM_018283.3:c.-152G>T (NUDT15) | NP_060753.1:n.-152G>T | |
NR_136687.1:n.29G>T (NUDT15) | ||
NR_136688.1:n.29G>T (NUDT15) |