HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183590670T>C , CM000663.2:g.183590670T>C | GRCh38 |
NC_000001.10:g.183559805T>C , CM000663.1:g.183559805T>C | GRCh37 |
NC_000001.9:g.181826428T>C | NCBI36 |
NG_007267.1:g.4912A>G , LRG_88:g.4912A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697330.1:c.-31+170A>G (NCF2) | ENSP00000513258.1:n.-31+170A>G | |
ENST00000697353.1:n.36A>G (NCF2) | ||
ENST00000367536.5:c.-31+170A>G (NCF2) | ENSP00000356506.1:n.-31+170A>G | |
ENST00000495321.1:n.234-7099T>C (SMG7) | ||
NM_001127651.2:c.-31+170A>G (NCF2) | NP_001121123.1:n.-31+170A>G | |
XM_011509580.1:c.-78A>G (NCF2) | XP_011507882.1:n.-78A>G | |
NM_001127651.3:c.-31+170A>G (NCF2) | NP_001121123.1:n.-31+170A>G |