HGVS | Genome Assembly |
---|---|
NC_000021.9:g.35301259C>G , CM000683.2:g.35301259C>G | GRCh38 |
NC_000021.8:g.36673557C>G , CM000683.1:g.36673557C>G | GRCh37 |
NC_000021.7:g.35595427C>G | NCBI36 |
NG_011402.2:g.688452G>C , LRG_482:g.688452G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000475045.6:c.-197+160702G>C | ENSP00000477072.1:n.-197+160702G>C |