Canonical Allele Identifier: CA823748351
Gene: HLA-F HGNC NCBI
HLA-F-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1189093818
gnomAD v3: 6-29729221-T-C
gnomAD v4: 6-29729221-T-C
MyVariant Identifiers: chr6:g.29696998T>C (hg19) chr6:g.29729221T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29729221T>C , CM000668.2:g.29729221T>C GRCh38
NC_000006.11:g.29696998T>C , CM000668.1:g.29696998T>C GRCh37
NC_000006.10:g.29804977T>C NCBI36
NG_012009.1:g.10882T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465459.2:c.403+3178T>C (HLA-F) ENSP00000486947.1:n.403+3178T>C
ENST00000475996.1:c.1375T>C (HLA-F)
NR_026972.1:n.1236-726A>G (HLA-F-AS1)
NR_026973.1:n.151-2082A>G (HLA-F-AS1)
XM_011514563.1:c.1003+3658T>C (HLA-F) XP_011512865.1:n.1003+3658T>C
XM_011514564.1:c.1003+3658T>C (HLA-F) XP_011512866.1:n.1003+3658T>C
XM_017010810.1:c.*1115T>C (HLA-F) XP_016866299.1:n.*1115T>C
XM_017010813.1:c.1158+2217T>C (HLA-F) XP_016866302.1:n.1158+2217T>C
XR_001743373.1:n.1188+2217T>C (HLA-F)
XR_001743374.1:n.1188+2217T>C (HLA-F)
XR_001743376.1:n.1131+2217T>C (HLA-F)
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