HGVS | Genome Assembly |
---|---|
NC_000003.12:g.10141558A>T , CM000665.2:g.10141558A>T | GRCh38 |
NC_000003.11:g.10183242A>T , CM000665.1:g.10183242A>T | GRCh37 |
NC_000003.10:g.10158242A>T | NCBI36 |
NG_008212.3:g.4924A>T , LRG_322:g.4924A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256474.2:c.-290A>T | ENSP00000256474.2:n.-290A>T |