HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102798291A>T , CM000673.2:g.102798291A>T | GRCh38 |
NC_000011.9:g.102669022A>T , CM000673.1:g.102669022A>T | GRCh37 |
NC_000011.8:g.102174232A>T | NCBI36 |
NG_011740.1:g.4945T>A | |
NG_011740.2:g.4945T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371455.7:n.423+169A>T | ||
ENST00000525739.6:n.682+169A>T | ||
ENST00000544704.1:n.443+169A>T | ||
NR_038390.1:n.682+169A>T |