HGVS | Genome Assembly |
---|---|
NC_000012.12:g.40197341T>C , CM000674.2:g.40197341T>C | GRCh38 |
NC_000012.11:g.40591143T>C , CM000674.1:g.40591143T>C | GRCh37 |
NC_000012.10:g.38877410T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000416796.5:c.-63+568T>C | ENSP00000398726.1:n.-63+568T>C |