HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6868357C>T , CM000673.2:g.6868357C>T | GRCh38 |
NC_000011.9:g.6889588C>T , CM000673.1:g.6889588C>T | GRCh37 |
NC_000011.8:g.6846164C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000641461.1:c.-132-1266C>T (OR10A2) MANE Select | ENSP00000493131.1:n.-132-1266C>T | |
XM_011520058.1:c.-436+29736G>A (OR2AG2) | XP_011518360.1:n.-436+29736G>A | |
XM_011520059.1:c.-436+29736G>A (OR2AG2) | XP_011518361.1:n.-436+29736G>A | |
XM_011520060.1:c.-436+29736G>A (OR2AG2) | XP_011518362.1:n.-436+29736G>A | |
XM_011520061.1:c.-436+56141G>A (OR2AG2) | XP_011518363.1:n.-436+56141G>A | |
NM_001004460.2:c.-132-1266C>T (OR10A2) MANE Select | NP_001004460.1:n.-132-1266C>T |