HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102798678T= , CM000673.2:g.102798678T= | GRCh38 |
NC_000011.9:g.102669409T= , CM000673.1:g.102669409T= | GRCh37 |
NC_000011.8:g.102174619T= | NCBI36 |
NG_011740.1:g.4558A= | |
NG_011740.2:g.4558A= |
HGVS | Amino-acid Change |
---|---|
NR_038390.1:n.682+556T= | |
ENST00000371455.7:n.423+556T= | |
ENST00000525739.6:n.682+556T= | |
ENST00000544704.1:n.443+556T= |