HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183590609G>T , CM000663.2:g.183590609G>T | GRCh38 |
NC_000001.10:g.183559744G>T , CM000663.1:g.183559744G>T | GRCh37 |
NC_000001.9:g.181826367G>T | NCBI36 |
NG_007267.1:g.4973C>A , LRG_88:g.4973C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697330.1:c.-31+231C>A (NCF2) | ENSP00000513258.1:n.-31+231C>A | |
ENST00000697353.1:n.83+14C>A (NCF2) | ||
ENST00000367536.5:c.-31+231C>A (NCF2) | ENSP00000356506.1:n.-31+231C>A | |
ENST00000495321.1:n.234-7160G>T (SMG7) | ||
NM_001127651.2:c.-31+231C>A (NCF2) | NP_001121123.1:n.-31+231C>A | |
XM_011509580.1:c.-31+14C>A (NCF2) | XP_011507882.1:n.-31+14C>A | |
NM_001127651.3:c.-31+231C>A (NCF2) | NP_001121123.1:n.-31+231C>A |