Canonical Allele Identifier: CA135985465

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs1005861367
• MyVariant Identifiers: chr6:g.29696816A>T (hg19) ; chr6:g.29729039A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729039A>T , CM000668.2:g.29729039A>T	GRCh38
NC_000006.11:g.29696816A>T , CM000668.1:g.29696816A>T	GRCh37
NC_000006.10:g.29804795A>T	NCBI36
NG_012009.1:g.10700A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000465459.2:c.403+2996A>T (HLA-F)	ENSP00000486947.1:n.403+2996A>T
ENST00000475996.1:c.1193A>T (HLA-F)
NR_026972.1:n.1236-544T>A (HLA-F-AS1)
NR_026973.1:n.151-1900T>A (HLA-F-AS1)
XM_011514563.1:c.1003+3476A>T (HLA-F)	XP_011512865.1:n.1003+3476A>T
XM_011514564.1:c.1003+3476A>T (HLA-F)	XP_011512866.1:n.1003+3476A>T
XM_017010810.1:c.*933A>T (HLA-F)	XP_016866299.1:n.*933A>T
XM_017010813.1:c.1158+2035A>T (HLA-F)	XP_016866302.1:n.1158+2035A>T
XR_001743373.1:n.1188+2035A>T (HLA-F)
XR_001743374.1:n.1188+2035A>T (HLA-F)
XR_001743376.1:n.1131+2035A>T (HLA-F)