Canonical Allele Identifier: CA823748388
Gene: HLA-F HGNC NCBI
HLA-F-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1337232461
gnomAD v3: 6-29729312-G-T
gnomAD v4: 6-29729312-G-T
MyVariant Identifiers: chr6:g.29697089G>T (hg19) chr6:g.29729312G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29729312G>T , CM000668.2:g.29729312G>T GRCh38
NC_000006.11:g.29697089G>T , CM000668.1:g.29697089G>T GRCh37
NC_000006.10:g.29805068G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000465459.2:c.403+3269G>T (HLA-F) ENSP00000486947.1:n.403+3269G>T
ENST00000475996.1:c.1466G>T (HLA-F)
NR_026972.1:n.1236-817C>A (HLA-F-AS1)
NR_026973.1:n.151-2173C>A (HLA-F-AS1)
XM_011514563.1:c.1003+3749G>T (HLA-F) XP_011512865.1:n.1003+3749G>T
XM_011514564.1:c.1003+3749G>T (HLA-F) XP_011512866.1:n.1003+3749G>T
XM_017010810.1:c.*1206G>T (HLA-F) XP_016866299.1:n.*1206G>T
XM_017010813.1:c.1158+2308G>T (HLA-F) XP_016866302.1:n.1158+2308G>T
XR_001743373.1:n.1188+2308G>T (HLA-F)
XR_001743374.1:n.1188+2308G>T (HLA-F)
XR_001743376.1:n.1131+2308G>T (HLA-F)
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