HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55063572G= , CM000663.2:g.55063572G= | GRCh38 |
NC_000001.10:g.55529245G= , CM000663.1:g.55529245G= | GRCh37 |
NC_000001.9:g.55301833G= | NCBI36 |
NG_009061.1:g.29026G= , LRG_275:g.29026G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.*407G= | ENSP00000501161.2:n.*407G= | |
ENST00000710286.1:c.2424G= | ENSP00000518176.1:p.Gln808= | |
ENST00000673903.1:c.1692G= | ENSP00000501257.1:p.Gln564= | |
ENST00000302118.5:c.2067G= MANE Select | ENSP00000303208.5:p.Gln689= | |
ENST00000490692.1:n.2613G= | ||
NM_174936.3:c.2067G= , LRG_275t1:c.2067G= | NP_777596.2:p.Gln689= | |
NR_110451.1:n.1674G= | ||
XM_011541193.1:c.1188G= | XP_011539495.1:p.Gln396= | |
NM_174936.4:c.2067G= MANE Select | NP_777596.2:p.Gln689= | |
NR_110451.2:n.1674G= |