HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50221293T>A , CM000684.2:g.50221293T>A | GRCh38 |
NC_000022.10:g.50659722T>A , CM000684.1:g.50659722T>A | GRCh37 |
NC_000022.9:g.49001849T>A | NCBI36 |
NG_032160.1:g.28679A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248846.10:c.3066A>T MANE Select | ENSP00000248846.5:p.Thr1022= | |
ENST00000248846.9:c.3066A>T | ENSP00000248846.5:p.Thr1022= | |
ENST00000439308.6:c.3066A>T | ENSP00000397387.2:p.Thr1022= | |
ENST00000491449.5:n.1373A>T | ||
ENST00000498611.5:n.3599A>T | ||
NM_020461.3:c.3066A>T | NP_065194.2:p.Thr1022= | |
XR_938347.1:n.3631A>T | ||
XR_938348.1:n.3049+735A>T | ||
XR_001755343.2:n.3635A>T | ||
XR_001755344.2:n.3635A>T | ||
XR_002958720.1:n.3053+735A>T | ||
XR_938347.2:n.3635A>T | ||
NM_020461.4:c.3066A>T MANE Select | NP_065194.3:p.Thr1022= |