HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183590698C>A , CM000663.2:g.183590698C>A | GRCh38 |
NC_000001.10:g.183559833C>A , CM000663.1:g.183559833C>A | GRCh37 |
NC_000001.9:g.181826456C>A | NCBI36 |
NG_007267.1:g.4884G>T , LRG_88:g.4884G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697330.1:c.-31+142G>T (NCF2) | ENSP00000513258.1:n.-31+142G>T | |
ENST00000697353.1:n.8G>T (NCF2) | ||
ENST00000367536.5:c.-31+142G>T (NCF2) | ENSP00000356506.1:n.-31+142G>T | |
ENST00000495321.1:n.234-7071C>A (SMG7) | ||
NM_001127651.2:c.-31+142G>T (NCF2) | NP_001121123.1:n.-31+142G>T | |
XM_011509580.1:c.-106G>T (NCF2) | XP_011507882.1:n.-106G>T | |
NM_001127651.3:c.-31+142G>T (NCF2) | NP_001121123.1:n.-31+142G>T |