HGVS | Genome Assembly |
---|---|
NC_000003.12:g.10141496T= , CM000665.2:g.10141496T= | GRCh38 |
NC_000003.11:g.10183180T= , CM000665.1:g.10183180T= | GRCh37 |
NC_000003.10:g.10158180T= | NCBI36 |
NG_008212.3:g.4862T= , LRG_322:g.4862T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256474.2:c.-352T= | ENSP00000256474.2:n.-352T= |