HGVS | Genome Assembly |
---|---|
NC_000012.12:g.64729051C= , CM000674.2:g.64729051C= | GRCh38 |
NC_000012.11:g.65122831C= , CM000674.1:g.65122831C= | GRCh37 |
NC_000012.10:g.63409098C= | NCBI36 |
NG_008955.1:g.35396G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258145.8:c.1105G= MANE Select | ENSP00000258145.3:p.Val369= | |
ENST00000258145.7:c.1105G= | ENSP00000258145.3:p.Val369= | |
ENST00000418919.6:c.937G= | ENSP00000413130.2:p.Val313= | |
ENST00000537823.1:n.104G= | ||
ENST00000540196.5:c.557-5938G= | ||
ENST00000540883.1:n.168G= | ||
ENST00000541781.5:n.1160G= | ||
ENST00000542058.5:c.1045G= | ENSP00000444819.1:p.Val349= | |
ENST00000543646.5:c.1201G= | ENSP00000438497.1:p.Val401= | |
NM_002076.3:c.1105G= | NP_002067.1:p.Val369= | |
NM_002076.4:c.1105G= MANE Select | NP_002067.1:p.Val369= |