HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992599C= , CM000667.2:g.177992599C= | GRCh38 |
NC_000005.9:g.177419600C= , CM000667.1:g.177419600C= | GRCh37 |
NC_000005.8:g.177352206C= | NCBI36 |
NG_015889.1:g.8644G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.*110G= MANE Select | ENSP00000311290.2:n.*110G= | |
NM_006261.4:c.*110G= | NP_006252.3:n.*110G= | |
NM_006261.5:c.*110G= MANE Select | NP_006252.4:n.*110G= |