HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52814297A>G , CM000674.2:g.52814297A>G | GRCh38 |
NC_000012.11:g.53208081A>G , CM000674.1:g.53208081A>G | GRCh37 |
NC_000012.10:g.51494348A>G | NCBI36 |
NG_007380.1:g.5255T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000551956.1:c.-239T>C | ENSP00000448220.1:n.-239T>C |