HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32276850T>C , CM000668.2:g.32276850T>C | GRCh38 |
NC_000006.11:g.32244627T>C , CM000668.1:g.32244627T>C | GRCh37 |
NC_000006.10:g.32352605T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011515039.1:c.421+14041T>C | XP_011513341.1:n.421+14041T>C | |
XM_011515040.1:c.421+14041T>C | XP_011513342.1:n.421+14041T>C | |
NR_136244.1:n.440+14041T>C | ||
NR_136245.1:n.242+21436T>C | ||
NR_136246.1:n.242+21436T>C |