HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989133T>A , CM000672.2:g.94989133T>A | GRCh38 |
NC_000010.10:g.96748890T>A , CM000672.1:g.96748890T>A | GRCh37 |
NC_000010.9:g.96738880T>A | NCBI36 |
NG_008385.1:g.55476T>A | |
NG_008385.2:g.55976T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.*105T>A MANE Select | ENSP00000260682.6:n.*105T>A | |
ENST00000643112.1:c.*587T>A | ENSP00000496202.1:n.*587T>A | |
ENST00000260682.6:c.*105T>A | ENSP00000260682.6:n.*105T>A | |
NM_000771.3:c.*105T>A | NP_000762.2:n.*105T>A | |
NM_000771.4:c.*105T>A MANE Select | NP_000762.2:n.*105T>A |