HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063563G= , CM000663.2:g.55063563G= | GRCh38 |
NC_000001.10:g.55529236G= , CM000663.1:g.55529236G= | GRCh37 |
NC_000001.9:g.55301824G= | NCBI36 |
NG_009061.1:g.29017G= , LRG_275:g.29017G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*398G= | ENSP00000501161.2:n.*398G= | |
ENST00000710286.1:c.2415G= | ENSP00000518176.1:p.Gln805= | |
ENST00000673903.1:c.1683G= | ENSP00000501257.1:p.Gln561= | |
ENST00000302118.5:c.2058G= MANE Select | ENSP00000303208.5:p.Gln686= | |
ENST00000490692.1:n.2604G= | ||
NM_174936.3:c.2058G= , LRG_275t1:c.2058G= | NP_777596.2:p.Gln686= | |
NR_110451.1:n.1665G= | ||
XM_011541193.1:c.1179G= | XP_011539495.1:p.Gln393= | |
NM_174936.4:c.2058G= MANE Select | NP_777596.2:p.Gln686= | |
NR_110451.2:n.1665G= |