Canonical Allele Identifier: CA2677953825

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354428-A-ACCCTCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354431_31354432insTCCCCCCCCCCCC , CM000668.2:g.31354431_31354432insTCCCCCCCCCCCC	GRCh38
NC_000006.11:g.31322208_31322209insTCCCCCCCCCCCC , CM000668.1:g.31322208_31322209insTCCCCCCCCCCCC	GRCh37
NC_000006.10:g.31430187_31430188insTCCCCCCCCCCCC	NCBI36
NG_023187.1:g.7784_7785insGGGGGGGGGAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+50_3140+51insGGGGGGGGGAGGG
ENST00000481849.6:n.3100+50_3100+51insGGGGGGGGGAGGG
ENST00000497377.6:n.3007+50_3007+51insGGGGGGGGGAGGG
ENST00000696558.1:c.1162+50_1162+51insGGGGGGGGGAGGG	ENSP00000512716.1:n.1162+50_1162+51insGGGGGGGGGAGGG
ENST00000696559.1:c.*4+50_*4+51insGGGGGGGGGAGGG	ENSP00000512717.1:n.*4+50_*4+51insGGGGGGGGGAGGG
ENST00000696560.1:c.*4+50_*4+51insGGGGGGGGGAGGG	ENSP00000512718.1:n.*4+50_*4+51insGGGGGGGGGAGGG
ENST00000696561.1:c.*4+50_*4+51insGGGGGGGGGAGGG	ENSP00000512719.1:n.*4+50_*4+51insGGGGGGGGGAGGG
ENST00000696562.1:c.*4+50_*4+51insGGGGGGGGGAGGG	ENSP00000512720.1:n.*4+50_*4+51insGGGGGGGGGAGGG
ENST00000412585.7:c.*4+50_*4+51insGGGGGGGGGAGGG MANE Select	ENSP00000399168.2:n.*4+50_*4+51insGGGGGGGGGAGGG
ENST00000412585.6:c.*4+50_*4+51insGGGGGGGGGAGGG	ENSP00000399168.2:n.*4+50_*4+51insGGGGGGGGGAGGG
ENST00000481849.5:n.328+50_328+51insGGGGGGGGGAGGG
ENST00000497377.5:n.492+50_492+51insGGGGGGGGGAGGG
NM_005514.6:c.*4+50_*4+51insGGGGGGGGGAGGG	NP_005505.2:n.*4+50_*4+51insGGGGGGGGGAGGG
XM_011514556.1:c.*4+50_*4+51insGGGGGGGGGAGGG	XP_011512858.1:n.*4+50_*4+51insGGGGGGGGGAGGG
XM_011514557.1:c.*4+50_*4+51insGGGGGGGGGAGGG	XP_011512859.1:n.*4+50_*4+51insGGGGGGGGGAGGG
XR_926175.1:n.1532+50_1532+51insGGGGGGGGGAGGG
NM_005514.7:c.*4+50_*4+51insGGGGGGGGGAGGG	NP_005505.2:n.*4+50_*4+51insGGGGGGGGGAGGG
NM_005514.8:c.*4+50_*4+51insGGGGGGGGGAGGG MANE Select	NP_005505.2:n.*4+50_*4+51insGGGGGGGGGAGGG