HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50220906C>A , CM000684.2:g.50220906C>A | GRCh38 |
NC_000022.10:g.50659335C>A , CM000684.1:g.50659335C>A | GRCh37 |
NC_000022.9:g.49001462C>A | NCBI36 |
NG_032160.1:g.29066G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248846.10:c.3453G>T MANE Select | ENSP00000248846.5:p.Val1151= | |
ENST00000248846.9:c.3453G>T | ENSP00000248846.5:p.Val1151= | |
ENST00000439308.6:c.3453G>T | ENSP00000397387.2:p.Val1151= | |
ENST00000491449.5:n.1760G>T | ||
ENST00000498611.5:n.3617+369G>T | ||
NM_020461.3:c.3453G>T | NP_065194.2:p.Val1151= | |
XR_938347.1:n.4018G>T | ||
XR_938348.1:n.3050-891G>T | ||
XR_001755343.2:n.4022G>T | ||
XR_001755344.2:n.4022G>T | ||
XR_002958720.1:n.3054-891G>T | ||
XR_938347.2:n.4022G>T | ||
NM_020461.4:c.3453G>T MANE Select | NP_065194.3:p.Val1151= |