HGVS | Genome Assembly |
---|---|
NC_000007.14:g.38021183T= , CM000669.2:g.38021183T= | GRCh38 |
NC_000007.13:g.38060785T= , CM000669.1:g.38060785T= | GRCh37 |
NC_000007.12:g.38027310T= | NCBI36 |
HGVS | Amino-acid Change |
---|---|
ENST00000447200.2:c.-53+4127A= | ENSP00000402262.2:n.-53+4127A= |
XR_001745170.1:n.832+7602T= | |
XR_927181.1:n.576+7602T= |