HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1103965A>C , CM000681.2:g.1103965A>C | GRCh38 |
NC_000019.9:g.1103964A>C , CM000681.1:g.1103964A>C | GRCh37 |
NC_000019.8:g.1054964A>C | NCBI36 |
NG_050621.1:g.5040A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000354171.12:c.-79A>C | ENSP00000346103.7:n.-79A>C | |
ENST00000616066.4:c.-79A>C | ENSP00000485000.1:n.-79A>C | |
NM_001039847.2:c.-79A>C | NP_001034936.1:n.-79A>C | |
NM_002085.4:c.-79A>C | NP_002076.2:n.-79A>C |