HGVS | Genome Assembly |
---|---|
NC_000004.12:g.54226459T>C , CM000666.2:g.54226459T>C | GRCh38 |
NC_000004.11:g.55092626T>C , CM000666.1:g.55092626T>C | GRCh37 |
NC_000004.10:g.54787383T>C | NCBI36 |
NG_009250.1:g.2363T>C , LRG_309:g.2363T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000507166.5:c.1018-48466T>C | ENSP00000423325.1:n.1018-48466T>C |