HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48037706C>A , CM000675.2:g.48037706C>A | GRCh38 |
NC_000013.10:g.48611842C>A , CM000675.1:g.48611842C>A | GRCh37 |
NC_000013.9:g.47509843C>A | NCBI36 |
NG_047021.1:g.5140C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643246.1:c.-263G>T (SUCLA2) | ENSP00000496235.1:n.-263G>T | |
ENST00000646804.1:c.-185G>T (SUCLA2) | ENSP00000493977.1:n.-185G>T | |
ENST00000258662.2:c.-41C>A (NUDT15) | ENSP00000258662.1:n.-41C>A | |
NM_001304745.1:c.-41C>A (NUDT15) | NP_001291674.1:n.-41C>A | |
NM_018283.2:c.-41C>A (NUDT15) | NP_060753.1:n.-41C>A | |
NM_018283.3:c.-41C>A (NUDT15) | NP_060753.1:n.-41C>A | |
NR_136687.1:n.140C>A (NUDT15) | ||
NR_136688.1:n.140C>A (NUDT15) |