HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135189T>A , CM000664.2:g.26135189T>A | GRCh38 |
NC_000002.11:g.26358058T>A , CM000664.1:g.26358058T>A | GRCh37 |
NC_000002.10:g.26211562T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*168T>A MANE Select | ENSP00000264710.4:n.*168T>A | |
ENST00000264710.4:c.*168T>A | ENSP00000264710.4:n.*168T>A | |
ENST00000495146.5:n.1134T>A | ||
NM_016131.4:c.*168T>A | NP_057215.3:n.*168T>A | |
XM_024452565.1:c.*168T>A | XP_024308333.1:n.*168T>A | |
NM_016131.5:c.*168T>A MANE Select | NP_057215.3:n.*168T>A |