Canonical Allele Identifier: CA1619118316

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766808694
• gnomAD v4: 6-31355169-A-ACAGCCAGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355174_31355182dup , CM000668.2:g.31355174_31355182dup	GRCh38
NC_000006.11:g.31322951_31322959dup , CM000668.1:g.31322951_31322959dup	GRCh37
NC_000006.10:g.31430930_31430938dup	NCBI36
NG_023187.1:g.7035_7043dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2988_2996dup
ENST00000481849.6:n.2507_2515dup
ENST00000497377.6:n.2414_2422dup
ENST00000640094.2:c.895+139_895+147dup	ENSP00000491275.2:n.895+139_895+147dup
ENST00000696558.1:c.1010_1018dup	ENSP00000512716.1:n.1010_1018dup
ENST00000696559.1:c.941_949dup	ENSP00000512717.1:p.Ala316_Val317insGlyLeuAla
ENST00000696560.1:c.941_949dup	ENSP00000512718.1:p.Ala316_Val317insGlyLeuAla
ENST00000696561.1:c.941_949dup	ENSP00000512719.1:p.Ala316_Val317insGlyLeuAla
ENST00000696562.1:c.941_949dup	ENSP00000512720.1:p.Ala316_Val317insGlyLeuAla
ENST00000412585.7:c.941_949dup MANE Select	ENSP00000399168.2:p.Ala316_Val317insGlyLeuAla
ENST00000640094.1:c.88+139_88+147dup	ENSP00000491275.1:n.88+139_88+147dup
ENST00000412585.6:c.941_949dup	ENSP00000399168.2:p.Ala316_Val317insGlyLeuAla
ENST00000463574.1:n.532_540dup
NM_005514.6:c.941_949dup	NP_005505.2:p.Ala316_Val317insGlyLeuAla
XM_011514556.1:c.974_982dup	XP_011512858.1:p.Ala327_Val328insGlyLeuAla
XM_011514557.1:c.895+139_895+147dup	XP_011512859.1:n.895+139_895+147dup
XR_926175.1:n.1380_1388dup
NM_005514.7:c.941_949dup	NP_005505.2:p.Ala316_Val317insGlyLeuAla
NM_005514.8:c.941_949dup MANE Select	NP_005505.2:p.Ala316_Val317insGlyLeuAla