HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6588563T>A , CM000668.2:g.6588563T>A | GRCh38 |
NC_000006.11:g.6588796T>A , CM000668.1:g.6588796T>A | GRCh37 |
NC_000006.10:g.6533795T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379953.6:c.-10+113T>A (LY86) | ENSP00000369286.1:n.-10+113T>A | |
NR_026970.1:n.196-19074A>T (LY86-AS1) |