HGVS | Genome Assembly |
---|---|
NC_000011.10:g.18018956A= , CM000673.2:g.18018956A= | GRCh38 |
NC_000011.9:g.18040503A= , CM000673.1:g.18040503A= | GRCh37 |
NC_000011.8:g.17997079A= | NCBI36 |
NG_011947.1:g.26833T= | |
NG_011947.2:g.26833T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682019.1:c.*2035T= MANE Select | ENSP00000508368.1:n.*2035T= | |
ENST00000250018.6:c.*2035T= | ENSP00000250018.2:n.*2035T= | |
NM_004179.3:c.*2035T= MANE Select | NP_004170.1:n.*2035T= |