HGVS | Genome Assembly |
---|---|
NC_000002.12:g.174765747G>C , CM000664.2:g.174765747G>C | GRCh38 |
NC_000002.11:g.175630475G>C , CM000664.1:g.175630475G>C | GRCh37 |
NC_000002.10:g.175338721G>C | NCBI36 |
NG_008172.1:g.3726C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000636168.2:c.-446-6114C>G | ENSP00000490338.2:n.-446-6114C>G |