HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50240216T>A , CM000684.2:g.50240216T>A | GRCh38 |
NC_000022.10:g.50678645T>A , CM000684.1:g.50678645T>A | GRCh37 |
NC_000022.9:g.49020772T>A | NCBI36 |
NG_032160.1:g.9756A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000248846.10:c.893A>T MANE Select | ENSP00000248846.5:p.Glu298Val | |
ENST00000248846.9:c.893A>T | ENSP00000248846.5:p.Glu298Val | |
ENST00000434349.1:c.136+9A>T | ||
ENST00000439308.6:c.893A>T | ENSP00000397387.2:p.Glu298Val | |
ENST00000498611.5:n.1426A>T | ||
NM_020461.3:c.893A>T | NP_065194.2:p.Glu298Val | |
XR_938347.1:n.1458A>T | ||
XR_938348.1:n.1458A>T | ||
XR_001755343.2:n.1462A>T | ||
XR_001755344.2:n.1462A>T | ||
XR_002958720.1:n.1462A>T | ||
XR_938347.2:n.1462A>T | ||
NM_020461.4:c.893A>T MANE Select | NP_065194.3:p.Glu298Val |