HGVS | Genome Assembly |
---|---|
NC_000002.12:g.127418299G>T , CM000664.2:g.127418299G>T | GRCh38 |
NC_000002.11:g.128175875G>T , CM000664.1:g.128175875G>T | GRCh37 |
NC_000002.10:g.127892345G>T | NCBI36 |
NG_016323.1:g.4880G>T , LRG_599:g.4880G>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_017004505.1:c.64G>T | XP_016859994.1:p.Gly22Trp | |
XM_024453002.1:c.64G>T | XP_024308770.1:p.Gly22Trp |