HGVS | Genome Assembly |
---|---|
NC_000012.12:g.53973689G>T , CM000674.2:g.53973689G>T | GRCh38 |
NC_000012.11:g.54367473G>T , CM000674.1:g.54367473G>T | GRCh37 |
NC_000012.10:g.52653740G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243082.4:c.448G>T (HOXC11) | ENSP00000243082.4:p.Ala150Ser | |
ENST00000546378.1:c.448G>T (HOXC11) MANE Select | ENSP00000446680.1:p.Ala150Ser | |
NM_014212.3:c.448G>T (HOXC11) | NP_055027.1:p.Ala150Ser | |
NR_047517.1:n.59+1209C>A (HOTAIR) | ||
NM_014212.4:c.448G>T (HOXC11) MANE Select | NP_055027.1:p.Ala150Ser |