HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58281011T>C , CM000679.2:g.58281011T>C | GRCh38 |
NC_000017.10:g.56358372T>C , CM000679.1:g.56358372T>C | GRCh37 |
NC_000017.9:g.53713371T>C | NCBI36 |
NG_009629.1:g.4925A>G , LRG_84:g.4925A>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_011524821.1:c.129A>G | XP_011523123.1:p.Pro43= | |
XM_011524823.1:c.129A>G | XP_011523125.1:p.Pro43= |