HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102798367A>G , CM000673.2:g.102798367A>G | GRCh38 |
NC_000011.9:g.102669098A>G , CM000673.1:g.102669098A>G | GRCh37 |
NC_000011.8:g.102174308A>G | NCBI36 |
NG_011740.1:g.4869T>C | |
NG_011740.2:g.4869T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371455.7:n.423+245A>G | ||
ENST00000525739.6:n.682+245A>G | ||
ENST00000544704.1:n.443+245A>G | ||
NR_038390.1:n.682+245A>G |