HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114213G>A , CM000667.2:g.140114213G>A | GRCh38 |
NC_000005.9:g.139493798G>A , CM000667.1:g.139493798G>A | GRCh37 |
NC_000005.8:g.139473982G>A | NCBI36 |
NG_041813.1:g.5091G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.32G>A MANE Select | ENSP00000332706.3:p.Gly11Asp | |
ENST00000505703.2:c.32G>A | ENSP00000498560.1:p.Gly11Asp | |
ENST00000651386.1:c.32G>A | ENSP00000499133.1:p.Gly11Asp | |
ENST00000331327.4:c.32G>A | ENSP00000332706.3:p.Gly11Asp | |
ENST00000502351.1:n.455G>A | ||
ENST00000505703.1:n.497G>A | ||
NM_005859.4:c.32G>A | NP_005850.1:p.Gly11Asp | |
NM_005859.5:c.32G>A MANE Select | NP_005850.1:p.Gly11Asp |