HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6588554G>T , CM000668.2:g.6588554G>T | GRCh38 |
NC_000006.11:g.6588787G>T , CM000668.1:g.6588787G>T | GRCh37 |
NC_000006.10:g.6533786G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379953.6:c.-10+104G>T (LY86) | ENSP00000369286.1:n.-10+104G>T | |
NR_026970.1:n.196-19065C>A (LY86-AS1) |