HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008153G>T , CM000666.2:g.88008153G>T | GRCh38 |
NC_000004.11:g.88929305G>T , CM000666.1:g.88929305G>T | GRCh37 |
NC_000004.10:g.89148329G>T | NCBI36 |
NG_008604.1:g.5486G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.420G>T MANE Select | ENSP00000237596.2:p.Gly140= | |
ENST00000237596.6:c.420G>T | ENSP00000237596.2:p.Gly140= | |
NM_000297.3:c.420G>T | NP_000288.1:p.Gly140= | |
XM_011532028.1:c.420G>T | XP_011530330.1:p.Gly140= | |
XR_244632.2:n.515G>T | ||
NR_156488.1:n.507G>T | ||
XM_011532028.2:c.420G>T | XP_011530330.1:p.Gly140= | |
NM_000297.4:c.420G>T MANE Select | NP_000288.1:p.Gly140= | |
NR_156488.2:n.519G>T |