HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071683T>A , CM000667.2:g.111071683T>A | GRCh38 |
NC_000005.9:g.110407381T>A , CM000667.1:g.110407381T>A | GRCh37 |
NC_000005.8:g.110435280T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000420978.6:c.34+166T>A | ENSP00000399099.2:n.34+166T>A | |
NR_045089.1:n.1438+166T>A | ||
NR_045089.2:n.1456+166T>A |