HGVS | Genome Assembly |
---|---|
NC_000003.12:g.36993316T>C , CM000665.2:g.36993316T>C | GRCh38 |
NC_000003.11:g.37034807T>C , CM000665.1:g.37034807T>C | GRCh37 |
NC_000003.10:g.37009811T>C | NCBI36 |
NG_007109.2:g.4967T>C , LRG_216:g.4967T>C | |
NG_008418.1:g.4989A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673673.2:c.-232T>C | ENSP00000500979.2:n.-232T>C |