HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1103980G>C , CM000681.2:g.1103980G>C | GRCh38 |
NC_000019.9:g.1103979G>C , CM000681.1:g.1103979G>C | GRCh37 |
NC_000019.8:g.1054979G>C | NCBI36 |
NG_050621.1:g.5055G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354171.12:c.-64G>C | ENSP00000346103.7:n.-64G>C | |
ENST00000616066.4:c.-64G>C | ENSP00000485000.1:n.-64G>C | |
NM_001039847.2:c.-64G>C | NP_001034936.1:n.-64G>C | |
NM_002085.4:c.-64G>C | NP_002076.2:n.-64G>C |