HGVS | Genome Assembly |
---|---|
NC_000003.12:g.36993310T>G , CM000665.2:g.36993310T>G | GRCh38 |
NC_000003.11:g.37034801T>G , CM000665.1:g.37034801T>G | GRCh37 |
NC_000003.10:g.37009805T>G | NCBI36 |
NG_007109.2:g.4961T>G , LRG_216:g.4961T>G | |
NG_008418.1:g.4995A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673673.2:c.-238T>G | ENSP00000500979.2:n.-238T>G |