Canonical Allele Identifier: CA1087461188

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31354618-A-ACCCCCCCC
• gnomAD v4: 6-31354618-A-ACCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354623_31354624insCCCCCCCC , CM000668.2:g.31354623_31354624insCCCCCCCC	GRCh38
NC_000006.11:g.31322400_31322401insCCCCCCCC , CM000668.1:g.31322400_31322401insCCCCCCCC	GRCh37
NC_000006.10:g.31430379_31430380insCCCCCCCC	NCBI36
NG_023187.1:g.7594_7595insGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+14_3092+15insGGGGGGGG
ENST00000481849.6:n.3052+14_3052+15insGGGGGGGG
ENST00000497377.6:n.2959+14_2959+15insGGGGGGGG
ENST00000640094.2:c.928+14_928+15insGGGGGGGG	ENSP00000491275.2:n.928+14_928+15insGGGGGGGG
ENST00000696558.1:c.1114+14_1114+15insGGGGGGGG	ENSP00000512716.1:n.1114+14_1114+15insGGGGGGGG
ENST00000696559.1:c.1045+14_1045+15insGGGGGGGG	ENSP00000512717.1:n.1045+14_1045+15insGGGGGGGG
ENST00000696560.1:c.1045+14_1045+15insGGGGGGGG	ENSP00000512718.1:n.1045+14_1045+15insGGGGGGGG
ENST00000696561.1:c.1045+14_1045+15insGGGGGGGG	ENSP00000512719.1:n.1045+14_1045+15insGGGGGGGG
ENST00000696562.1:c.1045+14_1045+15insGGGGGGGG	ENSP00000512720.1:n.1045+14_1045+15insGGGGGGGG
ENST00000412585.7:c.1045+14_1045+15insGGGGGGGG MANE Select	ENSP00000399168.2:n.1045+14_1045+15insGGGGGGGG
ENST00000640094.1:c.121+14_121+15insGGGGGGGG	ENSP00000491275.1:n.121+14_121+15insGGGGGGGG
ENST00000412585.6:c.1045+14_1045+15insGGGGGGGG	ENSP00000399168.2:n.1045+14_1045+15insGGGGGGGG
ENST00000481849.5:n.188_189insGGGGGGGG
ENST00000497377.5:n.444+14_444+15insGGGGGGGG
NM_005514.6:c.1045+14_1045+15insGGGGGGGG	NP_005505.2:n.1045+14_1045+15insGGGGGGGG
XM_011514556.1:c.1078+14_1078+15insGGGGGGGG	XP_011512858.1:n.1078+14_1078+15insGGGGGGGG
XM_011514557.1:c.928+14_928+15insGGGGGGGG	XP_011512859.1:n.928+14_928+15insGGGGGGGG
XR_926175.1:n.1484+14_1484+15insGGGGGGGG
NM_005514.7:c.1045+14_1045+15insGGGGGGGG	NP_005505.2:n.1045+14_1045+15insGGGGGGGG
NM_005514.8:c.1045+14_1045+15insGGGGGGGG MANE Select	NP_005505.2:n.1045+14_1045+15insGGGGGGGG