HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29737882A>G , CM000668.2:g.29737882A>G | GRCh38 |
NC_000006.11:g.29705659A>G , CM000668.1:g.29705659A>G | GRCh37 |
NC_000006.10:g.29813638A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465459.2:c.404-240A>G (HLA-F) | ENSP00000486947.1:n.404-240A>G | |
NR_026972.1:n.1235+84T>C (HLA-F-AS1) | ||
NR_026973.1:n.151-10743T>C (HLA-F-AS1) | ||
XM_011514563.1:c.1004-240A>G (HLA-F) | XP_011512865.1:n.1004-240A>G | |
XM_011514564.1:c.1004-240A>G (HLA-F) | XP_011512866.1:n.1004-240A>G | |
XM_017010813.1:c.1159-240A>G (HLA-F) | XP_016866302.1:n.1159-240A>G | |
XR_001743373.1:n.1189-240A>G (HLA-F) | ||
XR_001743374.1:n.1345-240A>G (HLA-F) | ||
XR_001743376.1:n.1288-240A>G (HLA-F) |