Canonical Allele Identifier: CA2677953558

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354363-C-CACCACACATTCGAAACGTCCCAATCAAAGGATCCCCATTACCTAGGCCTTTTCCCTCTGCCCCACCCCAGACCACTTCAGCTCCCCAGAATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354363_31354364insACCACACATTCGAAACGTCCCAATCAAAGGATCCCCATTACCTAGGCCTTTTCCCTCTGCCCCACCCCAGACCACTTCAGCTCCCCAGAATCT , CM000668.2:g.31354363_31354364insACCACACATTCGAAACGTCCCAATCAAAGGATCCCCATTACCTAGGCCTTTTCCCTCTGCCCCACCCCAGACCACTTCAGCTCCCCAGAATCT	GRCh38
NC_000006.11:g.31322140_31322141insACCACACATTCGAAACGTCCCAATCAAAGGATCCCCATTACCTAGGCCTTTTCCCTCTGCCCCACCCCAGACCACTTCAGCTCCCCAGAATCT , CM000668.1:g.31322140_31322141insACCACACATTCGAAACGTCCCAATCAAAGGATCCCCATTACCTAGGCCTTTTCCCTCTGCCCCACCCCAGACCACTTCAGCTCCCCAGAATCT	GRCh37
NC_000006.10:g.31430119_31430120insACCACACATTCGAAACGTCCCAATCAAAGGATCCCCATTACCTAGGCCTTTTCCCTCTGCCCCACCCCAGACCACTTCAGCTCCCCAGAATCT	NCBI36
NG_023187.1:g.7849_7850insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3141-68_3141-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT
ENST00000481849.6:n.3101-68_3101-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT
ENST00000497377.6:n.3008-68_3008-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT
ENST00000696558.1:c.1163-68_1163-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	ENSP00000512716.1:n.1163-68_1163-67insAGA...
ENST00000696559.1:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	ENSP00000512717.1:n.*5-68_*5-67insAGATTCT...
ENST00000696560.1:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	ENSP00000512718.1:n.*5-68_*5-67insAGATTCT...
ENST00000696561.1:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	ENSP00000512719.1:n.*5-68_*5-67insAGATTCT...
ENST00000696562.1:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	ENSP00000512720.1:n.*5-68_*5-67insAGATTCT...
ENST00000412585.7:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT MANE Select	ENSP00000399168.2:n.*5-68_*5-67insAGATTCT...
ENST00000412585.6:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	ENSP00000399168.2:n.*5-68_*5-67insAGATTCT...
ENST00000481849.5:n.329-68_329-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT
ENST00000497377.5:n.493-68_493-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT
NM_005514.6:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	NP_005505.2:n.*5-68_*5-67insAGATTCTGGGGAG...
XM_011514556.1:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	XP_011512858.1:n.*5-68_*5-67insAGATTCTGGG...
XM_011514557.1:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	XP_011512859.1:n.*5-68_*5-67insAGATTCTGGG...
XR_926175.1:n.1533-68_1533-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT
NM_005514.7:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT	NP_005505.2:n.*5-68_*5-67insAGATTCTGGGGAG...
NM_005514.8:c.*5-68_*5-67insAGATTCTGGGGAGCTGAAGTGGTCTGGGGTGGGGCAGAGGGAAAAGGCCTAGGTAATGGGGATCCTTTGATTGGGACGTTTCGAATGTGTGGT MANE Select	NP_005505.2:n.*5-68_*5-67insAGATTCTGGGGAG...