HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44313377C>G , CM000668.2:g.44313377C>G | GRCh38 |
NC_000006.11:g.44281114C>G , CM000668.1:g.44281114C>G | GRCh37 |
NC_000006.10:g.44389092C>G | NCBI36 |
NG_031952.1:g.4950G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000505802.1:c.855+5735C>G | ||
NM_001318876.2:c.946-128513C>G | NP_001305805.1:n.946-128513C>G |