HGVS | Genome Assembly |
---|---|
NC_000003.12:g.50345798G>A , CM000665.2:g.50345798G>A | GRCh38 |
NC_000003.11:g.50383229G>A , CM000665.1:g.50383229G>A | GRCh37 |
NC_000003.10:g.50358233G>A | NCBI36 |
NG_023270.1:g.139C>T | |
NG_042828.1:g.4949C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000231749.7:c.-219C>T | ENSP00000231749.3:n.-219C>T | |
XM_005265216.2:c.-347C>T | XP_005265273.1:n.-347C>T |