HGVS | Genome Assembly |
---|---|
NC_000008.11:g.95114879T>C , CM000670.2:g.95114879T>C | GRCh38 |
NC_000008.10:g.96127107T>C , CM000670.1:g.96127107T>C | GRCh37 |
NC_000008.9:g.96196283T>C | NCBI36 |
NG_016647.2:g.224609T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000523184.5:n.345-657T>C (NDUFAF6) | ||
XR_928428.1:n.362-657T>C (MIR3150BHG) | ||
NR_148913.1:n.1081-657T>C (NDUFAF6) | ||
NR_148914.1:n.1278-657T>C (NDUFAF6) | ||
NR_148913.2:n.1067-657T>C (NDUFAF6) | ||
NR_148914.2:n.1264-657T>C (NDUFAF6) |