HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34255221T>G , CM000679.2:g.34255221T>G | GRCh38 |
NC_000017.10:g.32582240T>G , CM000679.1:g.32582240T>G | GRCh37 |
NC_000017.9:g.29606353T>G | NCBI36 |
NG_012123.1:g.4945T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624362.1:n.4T>G |