HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140647633C>A , CM000667.2:g.140647633C>A | GRCh38 |
NC_000005.9:g.140027218C>A , CM000667.1:g.140027218C>A | GRCh37 |
NC_000005.8:g.140007402C>A | NCBI36 |
NG_021417.1:g.5153G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252102.8:c.-50G>T (NDUFA2) | ENSP00000252102.4:n.-50G>T | |
ENST00000502960.1:n.139G>T (NDUFA2) | ||
ENST00000512088.1:c.-50G>T (NDUFA2) | ENSP00000427220.1:n.-50G>T | |
ENST00000513256.5:c.4+324C>A (IK) | ENSP00000425564.1:n.4+324C>A | |
NM_001185012.1:c.-50G>T (NDUFA2) | NP_001171941.1:n.-50G>T | |
NM_002488.4:c.-50G>T (NDUFA2) | NP_002479.1:n.-50G>T | |
NR_033697.1:n.153G>T (NDUFA2) |