Canonical Allele Identifier: CA2677957886

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357079-C-CACTCACCGGCCCAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357093_31357094insAACTCACCGGCCCAG , CM000668.2:g.31357093_31357094insAACTCACCGGCCCAG	GRCh38
NC_000006.11:g.31324870_31324871insAACTCACCGGCCCAG , CM000668.1:g.31324870_31324871insAACTCACCGGCCCAG	GRCh37
NC_000006.10:g.31432849_31432850insAACTCACCGGCCCAG	NCBI36
NG_023187.1:g.5133_5134insTCTGGGCCGGTGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+6_1546+7insTCTGGGCCGGTGAGT
ENST00000481849.6:n.1546+6_1546+7insTCTGGGCCGGTGAGT
ENST00000497377.6:n.1546+6_1546+7insTCTGGGCCGGTGAGT
ENST00000640094.2:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000696558.1:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000696559.1:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000696560.1:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000696561.1:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000696562.1:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000412585.7:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000412585.6:c.73+6_73+7insTCTGGGCCGGTGAGT
ENST00000434333.1:c.-17_-16insTCTGGGCCGGTGAGT	ENSP00000405931.1:n.-17_-16insTCTGGGCCGGTGAGT
ENST00000498007.1:n.94+6_94+7insTCTGGGCCGGTGAGT
ENST00000603274.1:n.447_448insAACTCACCGGCCCAG
NM_005514.6:c.73+6_73+7insTCTGGGCCGGTGAGT
XM_011514557.1:c.73+6_73+7insTCTGGGCCGGTGAGT
XR_926175.1:n.83+6_83+7insTCTGGGCCGGTGAGT
NM_005514.7:c.73+6_73+7insTCTGGGCCGGTGAGT
NM_005514.8:c.73+6_73+7insTCTGGGCCGGTGAGT