HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322525C= , CM000677.2:g.73322525C= | GRCh38 |
NC_000015.9:g.73614866C= , CM000677.1:g.73614866C= | GRCh37 |
NC_000015.8:g.71401919C= | NCBI36 |
NG_009063.1:g.51740G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3568G= MANE Select | ENSP00000261917.3:p.Ala1190= | |
ENST00000261917.3:c.3568G= | ENSP00000261917.3:p.Ala1190= | |
NM_005477.2:c.3568G= | NP_005468.1:p.Ala1190= | |
XM_011521148.1:c.2350G= | XP_011519450.1:p.Ala784= | |
XM_011521148.2:c.2350G= | XP_011519450.1:p.Ala784= | |
NM_005477.3:c.3568G= MANE Select | NP_005468.1:p.Ala1190= |