HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583595T>C , CM000673.2:g.67583595T>C | GRCh38 |
NC_000011.9:g.67351066T>C , CM000673.1:g.67351066T>C | GRCh37 |
NC_000011.8:g.67107642T>C | NCBI36 |
NG_012075.1:g.5001T>C , LRG_723:g.5001T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398606.7:c.-249T>C | ENSP00000381607.3:n.-249T>C | |
NM_000852.3:c.-249T>C , LRG_723t1:c.-249T>C | NP_000843.1:n.-249T>C |