HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39965474T>A , CM000679.2:g.39965474T>A | GRCh38 |
NC_000017.10:g.38121727T>A , CM000679.1:g.38121727T>A | GRCh37 |
NC_000017.9:g.35375253T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301659.9:c.-5-209T>A MANE Select | ENSP00000301659.4:n.-5-209T>A | |
ENST00000635792.1:c.-5-209T>A | ENSP00000490739.1:n.-5-209T>A | |
ENST00000301659.8:c.-5-209T>A | ENSP00000301659.4:n.-5-209T>A | |
NM_178171.4:c.-5-209T>A | NP_835465.2:n.-5-209T>A | |
XM_017024502.2:c.-5-209T>A | XP_016879991.1:n.-5-209T>A | |
XM_017024503.1:c.-5-209T>A | XP_016879992.1:n.-5-209T>A | |
XM_017024504.2:c.-5-209T>A | XP_016879993.1:n.-5-209T>A | |
NM_178171.5:c.-5-209T>A MANE Select | NP_835465.2:n.-5-209T>A |