HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50220501A>G , CM000684.2:g.50220501A>G | GRCh38 |
NC_000022.10:g.50658930A>G , CM000684.1:g.50658930A>G | GRCh37 |
NC_000022.9:g.49001057A>G | NCBI36 |
NG_032160.1:g.29471T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248846.10:c.3858T>C MANE Select | ENSP00000248846.5:p.Ala1286= | |
ENST00000248846.9:c.3858T>C | ENSP00000248846.5:p.Ala1286= | |
ENST00000439308.6:c.3858T>C | ENSP00000397387.2:p.Ala1286= | |
ENST00000491449.5:n.2165T>C | ||
ENST00000498611.5:n.3618-486T>C | ||
NM_020461.3:c.3858T>C | NP_065194.2:p.Ala1286= | |
XR_938347.1:n.4423T>C | ||
XR_938348.1:n.3050-486T>C | ||
XR_001755343.2:n.4427T>C | ||
XR_001755344.2:n.4427T>C | ||
XR_002958720.1:n.3054-486T>C | ||
XR_938347.2:n.4427T>C | ||
NM_020461.4:c.3858T>C MANE Select | NP_065194.3:p.Ala1286= |