HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93588365A= , CM000672.2:g.93588365A= | GRCh38 |
NC_000010.10:g.95348122A= , CM000672.1:g.95348122A= | GRCh37 |
NC_000010.9:g.95338112A= | NCBI36 |
NG_032670.1:g.26701A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371481.9:c.*756A= MANE Select | ENSP00000360536.5:n.*756A= | |
ENST00000371481.8:c.*756A= | ENSP00000360536.4:n.*756A= | |
ENST00000371483.8:c.*756A= | ENSP00000360538.4:n.*756A= | |
ENST00000604414.1:c.696+12146A= | ENSP00000474477.1:n.696+12146A= | |
NM_001195755.1:c.*756A= | NP_001182684.1:n.*756A= | |
NM_181745.3:c.*756A= | NP_859529.2:n.*756A= | |
NM_001195755.2:c.*756A= MANE Select | NP_001182684.1:n.*756A= | |
NM_181745.4:c.*756A= | NP_859529.2:n.*756A= |