HGVS | Genome Assembly |
---|---|
NC_000002.12:g.203856932A= , CM000664.2:g.203856932A= | GRCh38 |
NC_000002.11:g.204721655A= , CM000664.1:g.204721655A= | GRCh37 |
NC_000002.10:g.204429900A= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696479.1:c.47+2856A= | ENSP00000512655.1:n.47+2856A= | |
XR_923797.1:n.225-5541A= |