HGVS | Genome Assembly |
---|---|
NC_000002.12:g.233250323T>G , CM000664.2:g.233250323T>G | GRCh38 |
NC_000002.11:g.234158969T>G , CM000664.1:g.234158969T>G | GRCh37 |
NC_000002.10:g.233823708T>G | NCBI36 |
NG_023038.1:g.3753T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000431917.5:c.-137-5779T>G | ENSP00000397512.1:n.-137-5779T>G |