HGVS | Genome Assembly |
---|---|
NC_000002.12:g.170814382T>C , CM000664.2:g.170814382T>C | GRCh38 |
NC_000002.11:g.171670892T>C , CM000664.1:g.171670892T>C | GRCh37 |
NC_000002.10:g.171379138T>C | NCBI36 |
NG_021477.1:g.2693T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000454603.5:c.-64+960T>C | ENSP00000402366.1:n.-64+960T>C | |
XM_011510922.1:c.-64+960T>C | XP_011509224.1:n.-64+960T>C |