HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2444917A>T , CM000673.2:g.2444917A>T | GRCh38 |
NC_000011.9:g.2466147A>T , CM000673.1:g.2466147A>T | GRCh37 |
NC_000011.8:g.2422723A>T | NCBI36 |
NG_008935.1:g.4927A>T , LRG_287:g.4927A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.23+209A>T | ENSP00000434560.2:n.23+209A>T | |
ENST00000496887.6:c.23+209A>T | ENSP00000434560.1:n.23+209A>T |