HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989089A= , CM000672.2:g.94989089A= | GRCh38 |
NC_000010.10:g.96748846A= , CM000672.1:g.96748846A= | GRCh37 |
NC_000010.9:g.96738836A= | NCBI36 |
NG_008385.1:g.55432A= | |
NG_008385.2:g.55932A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.*61A= MANE Select | ENSP00000260682.6:n.*61A= | |
ENST00000643112.1:c.*543A= | ENSP00000496202.1:n.*543A= | |
ENST00000260682.6:c.*61A= | ENSP00000260682.6:n.*61A= | |
NM_000771.3:c.*61A= | NP_000762.2:n.*61A= | |
NM_000771.4:c.*61A= MANE Select | NP_000762.2:n.*61A= |