HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989067G= , CM000672.2:g.94989067G= | GRCh38 |
NC_000010.10:g.96748824G= , CM000672.1:g.96748824G= | GRCh37 |
NC_000010.9:g.96738814G= | NCBI36 |
NG_008385.1:g.55410G= | |
NG_008385.2:g.55910G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.*39G= MANE Select | ENSP00000260682.6:n.*39G= | |
ENST00000643112.1:c.*521G= | ENSP00000496202.1:n.*521G= | |
ENST00000260682.6:c.*39G= | ENSP00000260682.6:n.*39G= | |
NM_000771.3:c.*39G= | NP_000762.2:n.*39G= | |
NM_000771.4:c.*39G= MANE Select | NP_000762.2:n.*39G= |