HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91111544C= , CM000674.2:g.91111544C= | GRCh38 |
NC_000012.11:g.91505321C= , CM000674.1:g.91505321C= | GRCh37 |
NC_000012.10:g.90029452C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.4:c.-168G= | ENSP00000266718.4:n.-168G= | |
NM_002345.3:c.-168G= | NP_002336.1:n.-168G= |