HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50220465A>T , CM000684.2:g.50220465A>T | GRCh38 |
NC_000022.10:g.50658894A>T , CM000684.1:g.50658894A>T | GRCh37 |
NC_000022.9:g.49001021A>T | NCBI36 |
NG_032160.1:g.29507T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248846.10:c.3894T>A MANE Select | ENSP00000248846.5:p.Pro1298= | |
ENST00000248846.9:c.3894T>A | ENSP00000248846.5:p.Pro1298= | |
ENST00000439308.6:c.3894T>A | ENSP00000397387.2:p.Pro1298= | |
ENST00000491449.5:n.2201T>A | ||
ENST00000498611.5:n.3618-450T>A | ||
NM_020461.3:c.3894T>A | NP_065194.2:p.Pro1298= | |
XR_938347.1:n.4459T>A | ||
XR_938348.1:n.3050-450T>A | ||
XR_001755343.2:n.4463T>A | ||
XR_001755344.2:n.4463T>A | ||
XR_002958720.1:n.3054-450T>A | ||
XR_938347.2:n.4463T>A | ||
NM_020461.4:c.3894T>A MANE Select | NP_065194.3:p.Pro1298= |