HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58281335A>G , CM000679.2:g.58281335A>G | GRCh38 |
NC_000017.10:g.56358696A>G , CM000679.1:g.56358696A>G | GRCh37 |
NC_000017.9:g.53713695A>G | NCBI36 |
NG_009629.1:g.4601T>C , LRG_84:g.4601T>C |
HGVS | Amino-acid change | |
---|---|---|
XM_011524821.1:c.71-266T>C | XP_011523123.1:n.71-266T>C | |
XM_011524823.1:c.71-266T>C | XP_011523125.1:n.71-266T>C |