HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992880G>A , CM000670.2:g.16992880G>A | GRCh38 |
NC_000008.10:g.16850389G>A , CM000670.1:g.16850389G>A | GRCh37 |
NC_000008.9:g.16894760G>A | NCBI36 |
NG_015978.1:g.14286C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*192C>T MANE Select | ENSP00000180166.5:n.*192C>T | |
ENST00000180166.5:c.*192C>T | ENSP00000180166.5:n.*192C>T | |
NM_019851.2:c.*192C>T | NP_062825.1:n.*192C>T | |
NM_019851.3:c.*192C>T MANE Select | NP_062825.1:n.*192C>T |