HGVS | Genome Assembly |
---|---|
NC_000002.12:g.148458751C= , CM000664.2:g.148458751C= | GRCh38 |
NC_000002.11:g.149216320C= , CM000664.1:g.149216320C= | GRCh37 |
NC_000002.10:g.148932790C= | NCBI36 |
NG_017003.1:g.442741C= | |
NG_017003.2:g.442741C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000637159.1:c.-8C= | ENSP00000490140.1:n.-8C= | |
ENST00000638043.2:c.-8C= | ENSP00000490728.2:n.-8C= | |
ENST00000642680.2:c.-8C= MANE Select | ENSP00000493871.2:n.-8C= | |
ENST00000404807.5:c.-8C= | ENSP00000384672.1:n.-8C= | |
ENST00000407073.5:c.-8C= | ENSP00000386049.1:n.-8C= | |
ENST00000627651.2:c.-8C= | ENSP00000486370.1:n.-8C= | |
ENST00000629878.2:c.-8C= | ENSP00000487089.1:n.-8C= | |
NM_018328.4:c.-8C= | NP_060798.2:n.-8C= | |
XM_005263711.2:c.-8C= | XP_005263768.1:n.-8C= | |
XM_011511470.1:c.-8C= | XP_011509772.1:n.-8C= | |
XM_011511471.1:c.-8C= | XP_011509773.1:n.-8C= | |
XM_011511472.1:c.-8C= | XP_011509774.1:n.-8C= | |
XM_011511473.1:c.-8C= | XP_011509775.1:n.-8C= | |
XM_011511474.1:c.-8C= | XP_011509776.1:n.-8C= | |
XM_011511475.1:c.-8C= | XP_011509777.1:n.-8C= | |
XM_011511476.1:c.-8C= | XP_011509778.1:n.-8C= | |
XR_922967.1:n.1222C= | ||
XM_011511470.2:c.-8C= | XP_011509772.1:n.-8C= | |
XM_011511472.2:c.-8C= | XP_011509774.1:n.-8C= | |
XM_024452987.1:c.-8C= | XP_024308755.1:n.-8C= | |
XM_024452988.1:c.-8C= | XP_024308756.1:n.-8C= | |
XM_024452989.1:c.-8C= | XP_024308757.1:n.-8C= | |
XM_024452990.1:c.-8C= | XP_024308758.1:n.-8C= | |
XR_002959318.1:n.305C= | ||
XR_002959319.1:n.305C= | ||
NM_001378120.1:c.-8C= MANE Select | NP_001365049.1:n.-8C= | |
NM_018328.5:c.-8C= | NP_060798.2:n.-8C= |