Canonical Allele Identifier: CA135985504

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs369127864
• gnomAD v2: 6-29696962-T-C
• gnomAD v3: 6-29729185-T-C
• gnomAD v4: 6-29729185-T-C
• MyVariant Identifiers: chr6:g.29696962T>C (hg19) ; chr6:g.29729185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729185T>C , CM000668.2:g.29729185T>C	GRCh38
NC_000006.11:g.29696962T>C , CM000668.1:g.29696962T>C	GRCh37
NC_000006.10:g.29804941T>C	NCBI36
NG_012009.1:g.10846T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465459.2:c.403+3142T>C (HLA-F)	ENSP00000486947.1:n.403+3142T>C
ENST00000475996.1:c.1339T>C (HLA-F)
NR_026972.1:n.1236-690A>G (HLA-F-AS1)
NR_026973.1:n.151-2046A>G (HLA-F-AS1)
XM_011514563.1:c.1003+3622T>C (HLA-F)	XP_011512865.1:n.1003+3622T>C
XM_011514564.1:c.1003+3622T>C (HLA-F)	XP_011512866.1:n.1003+3622T>C
XM_017010810.1:c.*1079T>C (HLA-F)	XP_016866299.1:n.*1079T>C
XM_017010813.1:c.1158+2181T>C (HLA-F)	XP_016866302.1:n.1158+2181T>C
XR_001743373.1:n.1188+2181T>C (HLA-F)
XR_001743374.1:n.1188+2181T>C (HLA-F)
XR_001743376.1:n.1131+2181T>C (HLA-F)