HGVS | Genome Assembly |
---|---|
NC_000001.11:g.220836896T>C , CM000663.2:g.220836896T>C | GRCh38 |
NC_000001.10:g.221010238T>C , CM000663.1:g.221010238T>C | GRCh37 |
NC_000001.9:g.219076861T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651706.1:c.842+31622T>C | ENSP00000499157.1:n.842+31622T>C | |
NR_046901.1:n.293-3704A>G |