HGVS | Genome Assembly |
---|---|
NC_000003.12:g.50345796C= , CM000665.2:g.50345796C= | GRCh38 |
NC_000003.11:g.50383227C= , CM000665.1:g.50383227C= | GRCh37 |
NC_000003.10:g.50358231C= | NCBI36 |
NG_023270.1:g.141G= | |
NG_042828.1:g.4951G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000231749.7:c.-217G= | ENSP00000231749.3:n.-217G= | |
XM_005265216.2:c.-345G= | XP_005265273.1:n.-345G= |