HGVS | Genome Assembly |
---|---|
NC_000010.11:g.102902701T>C , CM000672.2:g.102902701T>C | GRCh38 |
NC_000010.10:g.104662458T>C , CM000672.1:g.104662458T>C | GRCh37 |
NC_000010.9:g.104652448T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_017017027.1:c.447-2191A>G | XP_016872516.1:n.447-2191A>G | |
XR_001747577.1:n.169-2191A>G | ||
XR_001747578.1:n.345-2191A>G | ||
NR_160733.1:n.169-2191A>G |