Canonical Allele Identifier: CA3711259

Gene: HLA-B

Linked Data

• dbSNP Id: rs749494826
• ExAC: 6:31322910 G / GCAGCGACCA
• gnomAD v2: 6-31322910-G-GCAGCGACCA
• gnomAD v3: 6-31355133-G-GCAGCGACCA
• gnomAD v4: 6-31355133-G-GCAGCGACCA
• MyVariant Identifiers: chr6:g.31322910_31322911insCAGCGACCA (hg19) ; chr6:g.31355133_31355134insCAGCGACCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355138_31355146dup , CM000668.2:g.31355138_31355146dup	GRCh38
NC_000006.11:g.31322915_31322923dup , CM000668.1:g.31322915_31322923dup	GRCh37
NC_000006.10:g.31430894_31430902dup	NCBI36
NG_023187.1:g.7071_7079dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3024_3032dup
ENST00000481849.6:n.2543_2551dup
ENST00000497377.6:n.2450_2458dup
ENST00000640094.2:c.895+175_895+183dup	ENSP00000491275.2:n.895+175_895+183dup
ENST00000696558.1:c.1046_1054dup	ENSP00000512716.1:n.1046_1054dup
ENST00000696559.1:c.977_985dup	ENSP00000512717.1:p.Ala328_Ala329insValVa...
ENST00000696560.1:c.977_985dup	ENSP00000512718.1:p.Ala328_Ala329insValVa...
ENST00000696561.1:c.977_985dup	ENSP00000512719.1:p.Ala328_Ala329insValVa...
ENST00000696562.1:c.977_985dup	ENSP00000512720.1:p.Ala328_Ala329insValVa...
ENST00000412585.7:c.977_985dup MANE Select	ENSP00000399168.2:p.Ala328_Ala329insValVa...
ENST00000640094.1:c.88+175_88+183dup	ENSP00000491275.1:n.88+175_88+183dup
ENST00000412585.6:c.977_985dup	ENSP00000399168.2:p.Ala328_Ala329insValVa...
ENST00000463574.1:n.568_576dup
NM_005514.6:c.977_985dup	NP_005505.2:p.Ala328_Ala329insValValAla
XM_011514556.1:c.1010_1018dup	XP_011512858.1:p.Ala339_Ala340insValValAl...
XM_011514557.1:c.895+175_895+183dup	XP_011512859.1:n.895+175_895+183dup
XR_926175.1:n.1416_1424dup
NM_005514.7:c.977_985dup	NP_005505.2:p.Ala328_Ala329insValValAla
NM_005514.8:c.977_985dup MANE Select	NP_005505.2:p.Ala328_Ala329insValValAla