Canonical Allele Identifier: CA135985527

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs555267672
• gnomAD v2: 6-29697015-T-G
• gnomAD v3: 6-29729238-T-G
• gnomAD v4: 6-29729238-T-G
• MyVariant Identifiers: chr6:g.29697015T>G (hg19) ; chr6:g.29729238T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729238T>G , CM000668.2:g.29729238T>G	GRCh38
NC_000006.11:g.29697015T>G , CM000668.1:g.29697015T>G	GRCh37
NC_000006.10:g.29804994T>G	NCBI36
NG_012009.1:g.10899T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465459.2:c.403+3195T>G (HLA-F)	ENSP00000486947.1:n.403+3195T>G
ENST00000475996.1:c.1392T>G (HLA-F)
NR_026972.1:n.1236-743A>C (HLA-F-AS1)
NR_026973.1:n.151-2099A>C (HLA-F-AS1)
XM_011514563.1:c.1003+3675T>G (HLA-F)	XP_011512865.1:n.1003+3675T>G
XM_011514564.1:c.1003+3675T>G (HLA-F)	XP_011512866.1:n.1003+3675T>G
XM_017010810.1:c.*1132T>G (HLA-F)	XP_016866299.1:n.*1132T>G
XM_017010813.1:c.1158+2234T>G (HLA-F)	XP_016866302.1:n.1158+2234T>G
XR_001743373.1:n.1188+2234T>G (HLA-F)
XR_001743374.1:n.1188+2234T>G (HLA-F)
XR_001743376.1:n.1131+2234T>G (HLA-F)