HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183590684T>G , CM000663.2:g.183590684T>G | GRCh38 |
NC_000001.10:g.183559819T>G , CM000663.1:g.183559819T>G | GRCh37 |
NC_000001.9:g.181826442T>G | NCBI36 |
NG_007267.1:g.4898A>C , LRG_88:g.4898A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697330.1:c.-31+156A>C (NCF2) | ENSP00000513258.1:n.-31+156A>C | |
ENST00000697353.1:n.22A>C (NCF2) | ||
ENST00000367536.5:c.-31+156A>C (NCF2) | ENSP00000356506.1:n.-31+156A>C | |
ENST00000495321.1:n.234-7085T>G (SMG7) | ||
NM_001127651.2:c.-31+156A>C (NCF2) | NP_001121123.1:n.-31+156A>C | |
XM_011509580.1:c.-92A>C (NCF2) | XP_011507882.1:n.-92A>C | |
NM_001127651.3:c.-31+156A>C (NCF2) | NP_001121123.1:n.-31+156A>C |