HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47284374G= , CM000679.2:g.47284374G= | GRCh38 |
NC_000017.10:g.45361740G= , CM000679.1:g.45361740G= | GRCh37 |
NC_000017.9:g.42716739G= | NCBI36 |
NG_008332.2:g.35533G= , LRG_481:g.35533G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.362-69G= | ENSP00000513002.1:n.362-69G= | |
ENST00000559488.7:c.362-69G= MANE Select | ENSP00000452786.2:n.362-69G= | |
ENST00000559488.5:c.362-69G= | ENSP00000452786.1:n.362-69G= | |
ENST00000560629.1:c.327-69G= | ||
ENST00000571680.1:c.362-69G= | ENSP00000461626.1:n.362-69G= | |
NM_000212.2:c.362-69G= , LRG_481t1:c.362-69G= | NP_000203.2:n.362-69G= | |
NM_000212.3:c.362-69G= MANE Select | NP_000203.2:n.362-69G= |