HGVS | Genome Assembly |
---|---|
NC_000012.12:g.48966019G= , CM000674.2:g.48966019G= | GRCh38 |
NC_000012.11:g.49359802G= , CM000674.1:g.49359802G= | GRCh37 |
NC_000012.10:g.47646069G= | NCBI36 |
NG_023347.1:g.10840C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301061.9:c.*76C= MANE Select | ENSP00000301061.4:n.*76C= | |
ENST00000301061.8:c.*76C= | ENSP00000301061.4:n.*76C= | |
ENST00000403957.5:c.*528C= | ENSP00000385980.1:n.*528C= | |
ENST00000407467.5:c.*528C= | ENSP00000384691.1:n.*528C= | |
NM_003394.3:c.*76C= | NP_003385.2:n.*76C= | |
XM_011538721.1:c.*76C= | XP_011537023.1:n.*76C= | |
XM_011538722.1:c.*76C= | XP_011537024.1:n.*76C= | |
XM_017019919.1:c.*76C= | XP_016875408.1:n.*76C= | |
XM_024449179.1:c.*76C= | XP_024304947.1:n.*76C= | |
NM_003394.4:c.*76C= MANE Select | NP_003385.2:n.*76C= |