HGVS | Genome Assembly |
---|---|
NC_000004.12:g.102501253C>A , CM000666.2:g.102501253C>A | GRCh38 |
NC_000004.11:g.103422410C>A , CM000666.1:g.103422410C>A | GRCh37 |
NC_000004.10:g.103641442C>A | NCBI36 |
NG_050628.1:g.4925C>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011532467.1:c.639G>T | XP_011530769.1:p.Ala213= | |
NR_136202.1:n.48+1186G>T |