HGVS | Genome Assembly |
---|---|
NC_000011.10:g.113475451C>T , CM000673.2:g.113475451C>T | GRCh38 |
NC_000011.9:g.113346173C>T , CM000673.1:g.113346173C>T | GRCh37 |
NC_000011.8:g.112851383C>T | NCBI36 |
NG_008841.1:g.4829G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000540600.5:n.34+207G>A |