HGVS | Genome Assembly |
---|---|
NC_000002.12:g.170814263T>C , CM000664.2:g.170814263T>C | GRCh38 |
NC_000002.11:g.171670773T>C , CM000664.1:g.171670773T>C | GRCh37 |
NC_000002.10:g.171379019T>C | NCBI36 |
NG_021477.1:g.2574T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000454603.5:c.-64+841T>C | ENSP00000402366.1:n.-64+841T>C | |
XM_011510922.1:c.-64+841T>C | XP_011509224.1:n.-64+841T>C |