HGVS | Genome Assembly |
---|---|
NC_000012.12:g.53973936G>C , CM000674.2:g.53973936G>C | GRCh38 |
NC_000012.11:g.54367720G>C , CM000674.1:g.54367720G>C | GRCh37 |
NC_000012.10:g.52653987G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243082.4:c.686+9G>C (HOXC11) | ENSP00000243082.4:n.686+9G>C | |
ENST00000546378.1:c.682+13G>C (HOXC11) MANE Select | ENSP00000446680.1:n.682+13G>C | |
NM_014212.3:c.682+13G>C (HOXC11) | NP_055027.1:n.682+13G>C | |
NR_047517.1:n.59+962C>G (HOTAIR) | ||
NM_014212.4:c.682+13G>C (HOXC11) MANE Select | NP_055027.1:n.682+13G>C |