HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140647636T= , CM000667.2:g.140647636T= | GRCh38 |
NC_000005.9:g.140027221T= , CM000667.1:g.140027221T= | GRCh37 |
NC_000005.8:g.140007405T= | NCBI36 |
NG_021417.1:g.5150A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252102.8:c.-53A= (NDUFA2) | ENSP00000252102.4:n.-53A= | |
ENST00000502960.1:n.136A= (NDUFA2) | ||
ENST00000512088.1:c.-53A= (NDUFA2) | ENSP00000427220.1:n.-53A= | |
ENST00000513256.5:c.4+327T= (IK) | ENSP00000425564.1:n.4+327T= | |
NM_001185012.1:c.-53A= (NDUFA2) | NP_001171941.1:n.-53A= | |
NM_002488.4:c.-53A= (NDUFA2) | NP_002479.1:n.-53A= | |
NR_033697.1:n.150A= (NDUFA2) |