HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071636T>G , CM000667.2:g.111071636T>G | GRCh38 |
NC_000005.9:g.110407334T>G , CM000667.1:g.110407334T>G | GRCh37 |
NC_000005.8:g.110435233T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000420978.6:c.34+119T>G | ENSP00000399099.2:n.34+119T>G | |
NR_045089.1:n.1438+119T>G | ||
NR_045089.2:n.1456+119T>G |