HGVS | Genome Assembly |
---|---|
NC_000002.12:g.102355337T>C , CM000664.2:g.102355337T>C | GRCh38 |
NC_000002.11:g.102971797T>C , CM000664.1:g.102971797T>C | GRCh37 |
NC_000002.10:g.102338229T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000410040.5:c.-28-7296T>C | ENSP00000386663.1:n.-28-7296T>C |