Canonical Allele Identifier: CA565880058

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs906814200
• gnomAD v2: 6-29696775-A-AT
• gnomAD v3: 6-29728998-A-AT
• gnomAD v4: 6-29728998-A-AT
• MyVariant Identifiers: chr6:g.29696775_29696776insT (hg19) ; chr6:g.29728998_29728999insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729006dup , CM000668.2:g.29729006dup	GRCh38
NC_000006.11:g.29696783dup , CM000668.1:g.29696783dup	GRCh37
NC_000006.10:g.29804762dup	NCBI36
NG_012009.1:g.10667dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000465459.2:c.403+2963dup (HLA-F)	ENSP00000486947.1:n.403+2963dup
ENST00000475996.1:c.1160dup (HLA-F)
NR_026972.1:n.1236-504dup (HLA-F-AS1)
NR_026973.1:n.151-1860dup (HLA-F-AS1)
XM_011514563.1:c.1003+3443dup (HLA-F)	XP_011512865.1:n.1003+3443dup
XM_011514564.1:c.1003+3443dup (HLA-F)	XP_011512866.1:n.1003+3443dup
XM_017010810.1:c.*900dup (HLA-F)	XP_016866299.1:n.*900dup
XM_017010813.1:c.1158+2002dup (HLA-F)	XP_016866302.1:n.1158+2002dup
XR_001743373.1:n.1188+2002dup (HLA-F)
XR_001743374.1:n.1188+2002dup (HLA-F)
XR_001743376.1:n.1131+2002dup (HLA-F)