HGVS | Genome Assembly |
---|---|
NC_000009.12:g.97851907T>C , CM000671.2:g.97851907T>C | GRCh38 |
NC_000009.11:g.100614189T>C , CM000671.1:g.100614189T>C | GRCh37 |
NC_000009.10:g.99654010T>C | NCBI36 |
NG_011979.1:g.3653T>C |
HGVS | Amino-acid Change | |
---|---|---|
XR_930158.1:n.218+969A>G | ||
XR_930159.1:n.218+969A>G | ||
XR_930160.1:n.218+969A>G | ||
XR_930161.1:n.218+969A>G | ||
NR_147055.1:n.165+1009A>G |