HGVS | Genome Assembly |
---|---|
NC_000012.12:g.53973725G>C , CM000674.2:g.53973725G>C | GRCh38 |
NC_000012.11:g.54367509G>C , CM000674.1:g.54367509G>C | GRCh37 |
NC_000012.10:g.52653776G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243082.4:c.484G>C (HOXC11) | ENSP00000243082.4:p.Gly162Arg | |
ENST00000546378.1:c.484G>C (HOXC11) MANE Select | ENSP00000446680.1:p.Gly162Arg | |
NM_014212.3:c.484G>C (HOXC11) | NP_055027.1:p.Gly162Arg | |
NR_047517.1:n.59+1173C>G (HOTAIR) | ||
NM_014212.4:c.484G>C (HOXC11) MANE Select | NP_055027.1:p.Gly162Arg |