HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35797891T= , CM000668.2:g.35797891T= | GRCh38 |
NC_000006.11:g.35765668T= , CM000668.1:g.35765668T= | GRCh37 |
NC_000006.10:g.35873646T= | NCBI36 |
NG_012184.3:g.5686T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651132.1:c.-255+432T= | ENSP00000498322.1:n.-255+432T= | |
XM_011514403.1:c.-135+432T= | XP_011512705.1:n.-135+432T= |