HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1103945T>G , CM000681.2:g.1103945T>G | GRCh38 |
NC_000019.9:g.1103944T>G , CM000681.1:g.1103944T>G | GRCh37 |
NC_000019.8:g.1054944T>G | NCBI36 |
NG_050621.1:g.5020T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354171.12:c.-99T>G | ENSP00000346103.7:n.-99T>G | |
ENST00000616066.4:c.-99T>G | ENSP00000485000.1:n.-99T>G | |
NM_001039847.2:c.-99T>G | NP_001034936.1:n.-99T>G | |
NM_002085.4:c.-99T>G | NP_002076.2:n.-99T>G |