HGVS | Genome Assembly |
---|---|
NC_000007.14:g.148807263T= , CM000669.2:g.148807263T= | GRCh38 |
NC_000007.13:g.148504355T= , CM000669.1:g.148504355T= | GRCh37 |
NC_000007.12:g.148135288T= | NCBI36 |
NG_032043.1:g.82087A= , LRG_531:g.82087A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000683292.1:c.*1535A= | ENSP00000507503.1:n.*1535A= | |
XR_928101.1:n.515+2178T= | ||
XR_928102.1:n.722+2178T= |