HGVS | Genome Assembly |
---|---|
NC_000002.12:g.17933568C>T , CM000664.2:g.17933568C>T | GRCh38 |
NC_000002.11:g.18114835C>T , CM000664.1:g.18114835C>T | GRCh37 |
NC_000002.10:g.17978316C>T | NCBI36 |
NG_012873.1:g.59891C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000465292.5:n.305+15697C>T |