HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118304574T>C , CM000673.2:g.118304574T>C | GRCh38 |
NC_000011.9:g.118175289T>C , CM000673.1:g.118175289T>C | GRCh37 |
NC_000011.8:g.117680499T>C | NCBI36 |
NG_007383.1:g.4995T>C , LRG_38:g.4995T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.8:c.-262T>C | ENSP00000354566.4:n.-262T>C |