HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1103936T>C , CM000681.2:g.1103936T>C | GRCh38 |
NC_000019.9:g.1103935T>C , CM000681.1:g.1103935T>C | GRCh37 |
NC_000019.8:g.1054935T>C | NCBI36 |
NG_050621.1:g.5011T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000616066.4:c.-108T>C | ENSP00000485000.1:n.-108T>C | |
NM_001039847.2:c.-108T>C | NP_001034936.1:n.-108T>C | |
NM_002085.4:c.-108T>C | NP_002076.2:n.-108T>C |