HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652688C>A , CM000663.2:g.171652688C>A | GRCh38 |
NC_000001.10:g.171621828C>A , CM000663.1:g.171621828C>A | GRCh37 |
NC_000001.9:g.169888451C>A | NCBI36 |
NG_008859.1:g.4946G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.-77G>T MANE Select | ENSP00000037502.5:n.-77G>T | |
NM_000261.2:c.-77G>T MANE Select | NP_000252.1:n.-77G>T |