HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38811153T>C , CM000666.2:g.38811153T>C | GRCh38 |
NC_000004.11:g.38812774T>C , CM000666.1:g.38812774T>C | GRCh37 |
NC_000004.10:g.38489169T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-5960A>G | ENSP00000423725.1:n.-352-5960A>G |