HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992843A= , CM000670.2:g.16992843A= | GRCh38 |
NC_000008.10:g.16850352A= , CM000670.1:g.16850352A= | GRCh37 |
NC_000008.9:g.16894723A= | NCBI36 |
NG_015978.1:g.14323T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*229T= MANE Select | ENSP00000180166.5:n.*229T= | |
ENST00000180166.5:c.*229T= | ENSP00000180166.5:n.*229T= | |
NM_019851.2:c.*229T= | NP_062825.1:n.*229T= | |
NM_019851.3:c.*229T= MANE Select | NP_062825.1:n.*229T= |