Canonical Allele Identifier: CA565880216

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs1345496860
• gnomAD v2: 6-29697031-T-C
• gnomAD v3: 6-29729254-T-C
• gnomAD v4: 6-29729254-T-C
• MyVariant Identifiers: chr6:g.29697031T>C (hg19) ; chr6:g.29729254T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729254T>C , CM000668.2:g.29729254T>C	GRCh38
NC_000006.11:g.29697031T>C , CM000668.1:g.29697031T>C	GRCh37
NC_000006.10:g.29805010T>C	NCBI36
NG_012009.1:g.10915T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465459.2:c.403+3211T>C (HLA-F)	ENSP00000486947.1:n.403+3211T>C
ENST00000475996.1:c.1408T>C (HLA-F)
NR_026972.1:n.1236-759A>G (HLA-F-AS1)
NR_026973.1:n.151-2115A>G (HLA-F-AS1)
XM_011514563.1:c.1003+3691T>C (HLA-F)	XP_011512865.1:n.1003+3691T>C
XM_011514564.1:c.1003+3691T>C (HLA-F)	XP_011512866.1:n.1003+3691T>C
XM_017010810.1:c.*1148T>C (HLA-F)	XP_016866299.1:n.*1148T>C
XM_017010813.1:c.1158+2250T>C (HLA-F)	XP_016866302.1:n.1158+2250T>C
XR_001743373.1:n.1188+2250T>C (HLA-F)
XR_001743374.1:n.1188+2250T>C (HLA-F)
XR_001743376.1:n.1131+2250T>C (HLA-F)