HGVS | Genome Assembly |
---|---|
NC_000012.12:g.4381679A>C , CM000674.2:g.4381679A>C | GRCh38 |
NC_000012.11:g.4490845A>C , CM000674.1:g.4490845A>C | GRCh37 |
NC_000012.10:g.4361106A>C | NCBI36 |
NG_007087.1:g.3050T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648100.1:c.*1967+15397A>C | ENSP00000497536.1:n.*1967+15397A>C | |
ENST00000674624.1:c.*1204+15397A>C | ENSP00000501898.1:n.*1204+15397A>C |