Linked Data
dbSNP Id:
rs1810091824
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.95114712C>T , CM000670.2:g.95114712C>T | GRCh38 |
| NC_000008.10:g.96126940C>T , CM000670.1:g.96126940C>T | GRCh37 |
| NC_000008.9:g.96196116C>T | NCBI36 |
| NG_016647.2:g.224442C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000523184.5:n.345-824C>T (NDUFAF6) | ||
| XR_928428.1:n.362-824C>T (MIR3150BHG) | ||
| NR_148913.1:n.1081-824C>T (NDUFAF6) | ||
| NR_148914.1:n.1278-824C>T (NDUFAF6) | ||
| NR_148913.2:n.1067-824C>T (NDUFAF6) | ||
| NR_148914.2:n.1264-824C>T (NDUFAF6) |