HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35797496T= , CM000668.2:g.35797496T= | GRCh38 |
NC_000006.11:g.35765273T= , CM000668.1:g.35765273T= | GRCh37 |
NC_000006.10:g.35873251T= | NCBI36 |
NG_012184.3:g.5291T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651132.1:c.-255+37T= | ENSP00000498322.1:n.-255+37T= | |
XM_011514403.1:c.-135+37T= | XP_011512705.1:n.-135+37T= |