HGVS | Genome Assembly |
---|---|
NC_000001.11:g.220836660A>G , CM000663.2:g.220836660A>G | GRCh38 |
NC_000001.10:g.221010002A>G , CM000663.1:g.221010002A>G | GRCh37 |
NC_000001.9:g.219076625A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651706.1:c.842+31386A>G | ENSP00000499157.1:n.842+31386A>G | |
NR_046901.1:n.293-3468T>C |