Linked Data
dbSNP Id:
rs885945
gnomAD v2:
6-29696852-C-T
gnomAD v3:
6-29729075-C-T
gnomAD v4:
6-29729075-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29729075C>T , CM000668.2:g.29729075C>T | GRCh38 |
| NC_000006.11:g.29696852C>T , CM000668.1:g.29696852C>T | GRCh37 |
| NC_000006.10:g.29804831C>T | NCBI36 |
| NG_012009.1:g.10736C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000465459.2:c.403+3032C>T (HLA-F) | ENSP00000486947.1:n.403+3032C>T | |
| ENST00000475996.1:c.1229C>T (HLA-F) | ||
| NR_026972.1:n.1236-580G>A (HLA-F-AS1) | ||
| NR_026973.1:n.151-1936G>A (HLA-F-AS1) | ||
| XM_011514563.1:c.1003+3512C>T (HLA-F) | XP_011512865.1:n.1003+3512C>T | |
| XM_011514564.1:c.1003+3512C>T (HLA-F) | XP_011512866.1:n.1003+3512C>T | |
| XM_017010810.1:c.*969C>T (HLA-F) | XP_016866299.1:n.*969C>T | |
| XM_017010813.1:c.1158+2071C>T (HLA-F) | XP_016866302.1:n.1158+2071C>T | |
| XR_001743373.1:n.1188+2071C>T (HLA-F) | ||
| XR_001743374.1:n.1188+2071C>T (HLA-F) | ||
| XR_001743376.1:n.1131+2071C>T (HLA-F) |