HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154379421G= , CM000685.2:g.154379421G= | GRCh38 |
NC_000023.10:g.153607781G= , CM000685.1:g.153607781G= | GRCh37 |
NC_000023.9:g.153260975G= | NCBI36 |
NG_008677.1:g.9986G= , LRG_745:g.9986G= | |
NG_011506.1:g.226C= | |
NG_011506.2:g.218C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682114.1:c.-64G= | ENSP00000507245.1:n.-64G= | |
ENST00000369842.9:c.-64G= MANE Select | ENSP00000358857.4:n.-64G= | |
ENST00000369835.3:c.-64G= | ENSP00000358850.3:n.-64G= | |
ENST00000369842.8:c.-64G= | ENSP00000358857.4:n.-64G= | |
ENST00000428228.5:c.-64G= | ENSP00000401081.1:n.-64G= | |
ENST00000485261.1:n.18G= | ||
ENST00000486738.5:n.81G= | ||
NM_000117.2:c.-64G= , LRG_745t1:c.-64G= | NP_000108.1:n.-64G= | |
XM_024452349.1:c.-272G= | XP_024308117.1:n.-272G= | |
NM_000117.3:c.-64G= MANE Select | NP_000108.1:n.-64G= |