Canonical Allele Identifier: CA2677953545

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354362-C-CTCACCACACATTCGAAACGTCCCTATCAAAGGATCCCCATTACCTAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354362_31354363insTCACCACACATTCGAAACGTCCCTATCAAAGGATCCCCATTACCTAGG , CM000668.2:g.31354362_31354363insTCACCACACATTCGAAACGTCCCTATCAAAGGATCCCCATTACCTAGG	GRCh38
NC_000006.11:g.31322139_31322140insTCACCACACATTCGAAACGTCCCTATCAAAGGATCCCCATTACCTAGG , CM000668.1:g.31322139_31322140insTCACCACACATTCGAAACGTCCCTATCAAAGGATCCCCATTACCTAGG	GRCh37
NC_000006.10:g.31430118_31430119insTCACCACACATTCGAAACGTCCCTATCAAAGGATCCCCATTACCTAGG	NCBI36
NG_023187.1:g.7850_7851insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3141-67_3141-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA
ENST00000481849.6:n.3101-67_3101-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA
ENST00000497377.6:n.3008-67_3008-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA
ENST00000696558.1:c.1163-67_1163-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	ENSP00000512716.1:n.1163-67_1163-66insCCT...
ENST00000696559.1:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	ENSP00000512717.1:n.*5-67_*5-66insCCTAGGT...
ENST00000696560.1:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	ENSP00000512718.1:n.*5-67_*5-66insCCTAGGT...
ENST00000696561.1:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	ENSP00000512719.1:n.*5-67_*5-66insCCTAGGT...
ENST00000696562.1:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	ENSP00000512720.1:n.*5-67_*5-66insCCTAGGT...
ENST00000412585.7:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA MANE Select	ENSP00000399168.2:n.*5-67_*5-66insCCTAGGT...
ENST00000412585.6:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	ENSP00000399168.2:n.*5-67_*5-66insCCTAGGT...
ENST00000481849.5:n.329-67_329-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA
ENST00000497377.5:n.493-67_493-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA
NM_005514.6:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	NP_005505.2:n.*5-67_*5-66insCCTAGGTAATGGG...
XM_011514556.1:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	XP_011512858.1:n.*5-67_*5-66insCCTAGGTAAT...
XM_011514557.1:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	XP_011512859.1:n.*5-67_*5-66insCCTAGGTAAT...
XR_926175.1:n.1533-67_1533-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA
NM_005514.7:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA	NP_005505.2:n.*5-67_*5-66insCCTAGGTAATGGG...
NM_005514.8:c.*5-67_*5-66insCCTAGGTAATGGGGATCCTTTGATAGGGACGTTTCGAATGTGTGGTGA MANE Select	NP_005505.2:n.*5-67_*5-66insCCTAGGTAATGGG...