HGVS | Genome Assembly |
---|---|
NC_000003.12:g.36993338T= , CM000665.2:g.36993338T= | GRCh38 |
NC_000003.11:g.37034829T= , CM000665.1:g.37034829T= | GRCh37 |
NC_000003.10:g.37009833T= | NCBI36 |
NG_007109.2:g.4989T= , LRG_216:g.4989T= | |
NG_008418.1:g.4967A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673673.2:c.-210T= | ENSP00000500979.2:n.-210T= | |
ENST00000231790.6:c.-210T= | ENSP00000231790.2:n.-210T= |