HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62631582T= , CM000672.2:g.62631582T= | GRCh38 |
NC_000010.10:g.64391342T= , CM000672.1:g.64391342T= | GRCh37 |
NC_000010.9:g.64061348T= | NCBI36 |
NG_021209.1:g.262427T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647733.1:c.1129+8332T= | ENSP00000502188.1:n.1129+8332T= | |
ENST00000395251.5:c.-184-12160T= | ENSP00000378672.1:n.-184-12160T= | |
ENST00000410046.7:c.1129+8332T= | ENSP00000387091.3:n.1129+8332T= | |
NM_199451.2:c.1129+8332T= | NP_955523.1:n.1129+8332T= | |
NM_199452.3:c.-184-12160T= | NP_955524.3:n.-184-12160T= | |
XR_946002.1:n.82-6459A= | ||
XR_946002.2:n.82-6459A= | ||
NM_199451.3:c.1129+8332T= | NP_955523.1:n.1129+8332T= |