Linked Data
gnomAD v4:
5-140647632-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140647632C>T , CM000667.2:g.140647632C>T | GRCh38 |
| NC_000005.9:g.140027217C>T , CM000667.1:g.140027217C>T | GRCh37 |
| NC_000005.8:g.140007401C>T | NCBI36 |
| NG_021417.1:g.5154G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252102.8:c.-49G>A (NDUFA2) | ENSP00000252102.4:n.-49G>A | |
| ENST00000502960.1:n.140G>A (NDUFA2) | ||
| ENST00000512088.1:c.-49G>A (NDUFA2) | ENSP00000427220.1:n.-49G>A | |
| ENST00000513256.5:c.4+323C>T (IK) | ENSP00000425564.1:n.4+323C>T | |
| NM_001185012.1:c.-49G>A (NDUFA2) | NP_001171941.1:n.-49G>A | |
| NM_002488.4:c.-49G>A (NDUFA2) | NP_002479.1:n.-49G>A | |
| NR_033697.1:n.154G>A (NDUFA2) |