HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102799093A= , CM000673.2:g.102799093A= | GRCh38 |
NC_000011.9:g.102669824A= , CM000673.1:g.102669824A= | GRCh37 |
NC_000011.8:g.102175034A= | NCBI36 |
NG_011740.1:g.4143T= | |
NG_011740.2:g.4143T= |
HGVS | Amino-acid Change |
---|---|
NR_038390.1:n.682+971A= | |
ENST00000371455.7:n.423+971A= | |
ENST00000525739.6:n.682+971A= | |
ENST00000544704.1:n.443+971A= |