Canonical Allele Identifier: CA566689315

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31322240-A-ACCCCCCCCCCCC
• MyVariant Identifiers: chr6:g.31322240_31322241insCCCCCCCCCCCC (hg19) ; chr6:g.31354463_31354464insCCCCCCCCCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354467_31354468insCCCCCCCCCCCC , CM000668.2:g.31354467_31354468insCCCCCCCCCCCC	GRCh38
NC_000006.11:g.31322244_31322245insCCCCCCCCCCCC , CM000668.1:g.31322244_31322245insCCCCCCCCCCCC	GRCh37
NC_000006.10:g.31430223_31430224insCCCCCCCCCCCC	NCBI36
NG_023187.1:g.7749_7750insGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+15_3140+16insGGGGGGGGGGGG
ENST00000481849.6:n.3100+15_3100+16insGGGGGGGGGGGG
ENST00000497377.6:n.3007+15_3007+16insGGGGGGGGGGGG
ENST00000696558.1:c.1162+15_1162+16insGGGGGGGGGGGG	ENSP00000512716.1:n.1162+15_1162+16insGGGGGGGGGGGG
ENST00000696559.1:c.*4+15_*4+16insGGGGGGGGGGGG	ENSP00000512717.1:n.*4+15_*4+16insGGGGGGGGGGGG
ENST00000696560.1:c.*4+15_*4+16insGGGGGGGGGGGG	ENSP00000512718.1:n.*4+15_*4+16insGGGGGGGGGGGG
ENST00000696561.1:c.*4+15_*4+16insGGGGGGGGGGGG	ENSP00000512719.1:n.*4+15_*4+16insGGGGGGGGGGGG
ENST00000696562.1:c.*4+15_*4+16insGGGGGGGGGGGG	ENSP00000512720.1:n.*4+15_*4+16insGGGGGGGGGGGG
ENST00000412585.7:c.*4+15_*4+16insGGGGGGGGGGGG MANE Select	ENSP00000399168.2:n.*4+15_*4+16insGGGGGGGGGGGG
ENST00000412585.6:c.*4+15_*4+16insGGGGGGGGGGGG	ENSP00000399168.2:n.*4+15_*4+16insGGGGGGGGGGGG
ENST00000481849.5:n.328+15_328+16insGGGGGGGGGGGG
ENST00000497377.5:n.492+15_492+16insGGGGGGGGGGGG
NM_005514.6:c.*4+15_*4+16insGGGGGGGGGGGG	NP_005505.2:n.*4+15_*4+16insGGGGGGGGGGGG
XM_011514556.1:c.*4+15_*4+16insGGGGGGGGGGGG	XP_011512858.1:n.*4+15_*4+16insGGGGGGGGGGGG
XM_011514557.1:c.*4+15_*4+16insGGGGGGGGGGGG	XP_011512859.1:n.*4+15_*4+16insGGGGGGGGGGGG
XR_926175.1:n.1532+15_1532+16insGGGGGGGGGGGG
NM_005514.7:c.*4+15_*4+16insGGGGGGGGGGGG	NP_005505.2:n.*4+15_*4+16insGGGGGGGGGGGG
NM_005514.8:c.*4+15_*4+16insGGGGGGGGGGGG MANE Select	NP_005505.2:n.*4+15_*4+16insGGGGGGGGGGGG