HGVS | Genome Assembly |
---|---|
NC_000012.12:g.1529005A>C , CM000674.2:g.1529005A>C | GRCh38 |
NC_000012.11:g.1638171A>C , CM000674.1:g.1638171A>C | GRCh37 |
NC_000012.10:g.1508432A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_017020292.2:c.*835T>G | XP_016875781.1:n.*835T>G | |
NR_160736.1:n.2854T>G |