HGVS | Genome Assembly |
---|---|
NC_000017.11:g.56594428C= , CM000679.2:g.56594428C= | GRCh38 |
NC_000017.10:g.54671789C= , CM000679.1:g.54671789C= | GRCh37 |
NC_000017.9:g.52026788C= | NCBI36 |
NG_011958.1:g.5730C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332822.6:c.205C= MANE Select | ENSP00000328181.4:p.Leu69= | |
ENST00000332822.4:c.205C= | ENSP00000328181.4:p.Leu69= | |
NM_005450.4:c.205C= | NP_005441.1:p.Leu69= | |
NM_005450.6:c.205C= MANE Select | NP_005441.1:p.Leu69= |