Canonical Allele Identifier: CA135985464

Gene: HLA-F HLA-F-AS1

Linked Data

• dbSNP Id: rs557309917
• gnomAD v4: 6-29729033-T-C
• MyVariant Identifiers: chr6:g.29696810T>C (hg19) ; chr6:g.29729033T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29729033T>C , CM000668.2:g.29729033T>C	GRCh38
NC_000006.11:g.29696810T>C , CM000668.1:g.29696810T>C	GRCh37
NC_000006.10:g.29804789T>C	NCBI36
NG_012009.1:g.10694T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000465459.2:c.403+2990T>C (HLA-F)	ENSP00000486947.1:n.403+2990T>C
ENST00000475996.1:c.1187T>C (HLA-F)
NR_026972.1:n.1236-538A>G (HLA-F-AS1)
NR_026973.1:n.151-1894A>G (HLA-F-AS1)
XM_011514563.1:c.1003+3470T>C (HLA-F)	XP_011512865.1:n.1003+3470T>C
XM_011514564.1:c.1003+3470T>C (HLA-F)	XP_011512866.1:n.1003+3470T>C
XM_017010810.1:c.*927T>C (HLA-F)	XP_016866299.1:n.*927T>C
XM_017010813.1:c.1158+2029T>C (HLA-F)	XP_016866302.1:n.1158+2029T>C
XR_001743373.1:n.1188+2029T>C (HLA-F)
XR_001743374.1:n.1188+2029T>C (HLA-F)
XR_001743376.1:n.1131+2029T>C (HLA-F)