Canonical Allele Identifier: CA565880060

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs1000094516
• gnomAD v2: 6-29696785-G-T
• gnomAD v3: 6-29729008-G-T
• gnomAD v4: 6-29729008-G-T
• MyVariant Identifiers: chr6:g.29696785G>T (hg19) ; chr6:g.29729008G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729008G>T , CM000668.2:g.29729008G>T	GRCh38
NC_000006.11:g.29696785G>T , CM000668.1:g.29696785G>T	GRCh37
NC_000006.10:g.29804764G>T	NCBI36
NG_012009.1:g.10669G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000465459.2:c.403+2965G>T (HLA-F)	ENSP00000486947.1:n.403+2965G>T
ENST00000475996.1:c.1162G>T (HLA-F)
NR_026972.1:n.1236-513C>A (HLA-F-AS1)
NR_026973.1:n.151-1869C>A (HLA-F-AS1)
XM_011514563.1:c.1003+3445G>T (HLA-F)	XP_011512865.1:n.1003+3445G>T
XM_011514564.1:c.1003+3445G>T (HLA-F)	XP_011512866.1:n.1003+3445G>T
XM_017010810.1:c.*902G>T (HLA-F)	XP_016866299.1:n.*902G>T
XM_017010813.1:c.1158+2004G>T (HLA-F)	XP_016866302.1:n.1158+2004G>T
XR_001743373.1:n.1188+2004G>T (HLA-F)
XR_001743374.1:n.1188+2004G>T (HLA-F)
XR_001743376.1:n.1131+2004G>T (HLA-F)