HGVS | Genome Assembly |
---|---|
NC_000016.10:g.176897A= , CM000678.2:g.176897A= | GRCh38 |
NC_000016.9:g.226896A= , CM000678.1:g.226896A= | GRCh37 |
NC_000016.8:g.166896A= | NCBI36 |
NG_000006.1:g.37760A= | |
NG_059186.1:g.5247A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320868.9:c.96-32A= MANE Select | ENSP00000322421.5:n.96-32A= | |
ENST00000397797.1:c.-1-32A= | ENSP00000380899.1:n.-1-32A= | |
ENST00000472694.1:n.200A= | ||
ENST00000487791.1:n.65-32A= | ||
NM_000558.4:c.96-32A= | NP_000549.1:n.96-32A= | |
NM_000558.5:c.96-32A= MANE Select | NP_000549.1:n.96-32A= |