HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6588565T>C , CM000668.2:g.6588565T>C | GRCh38 |
NC_000006.11:g.6588798T>C , CM000668.1:g.6588798T>C | GRCh37 |
NC_000006.10:g.6533797T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379953.6:c.-10+115T>C (LY86) | ENSP00000369286.1:n.-10+115T>C | |
NR_026970.1:n.196-19076A>G (LY86-AS1) |