HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52814333A>G , CM000674.2:g.52814333A>G | GRCh38 |
NC_000012.11:g.53208117A>G , CM000674.1:g.53208117A>G | GRCh37 |
NC_000012.10:g.51494384A>G | NCBI36 |
NG_007380.1:g.5219T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000551956.1:c.-275T>C | ENSP00000448220.1:n.-275T>C |