Canonical Allele Identifier: CA2677956855
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31356376-T-TACCCGCGGAGGAGGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356376_31356377insACCCGCGGAGGAGGC , CM000668.2:g.31356376_31356377insACCCGCGGAGGAGGC GRCh38
NC_000006.11:g.31324153_31324154insACCCGCGGAGGAGGC , CM000668.1:g.31324153_31324154insACCCGCGGAGGAGGC GRCh37
NC_000006.10:g.31432132_31432133insACCCGCGGAGGAGGC NCBI36
NG_023187.1:g.5836_5837insGCCTCCTCCGCGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1882_1883insGCCTCCTCCGCGGGT
ENST00000481849.6:n.1882_1883insGCCTCCTCCGCGGGT
ENST00000497377.6:n.1882_1883insGCCTCCTCCGCGGGT
ENST00000640094.2:c.409_410insGCCTCCTCCGCGGGT ENSP00000491275.2:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000696558.1:c.409_410insGCCTCCTCCGCGGGT ENSP00000512716.1:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000696559.1:c.409_410insGCCTCCTCCGCGGGT ENSP00000512717.1:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000696560.1:c.409_410insGCCTCCTCCGCGGGT ENSP00000512718.1:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000696561.1:c.409_410insGCCTCCTCCGCGGGT ENSP00000512719.1:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000696562.1:c.409_410insGCCTCCTCCGCGGGT ENSP00000512720.1:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000412585.7:c.409_410insGCCTCCTCCGCGGGT MANE Select ENSP00000399168.2:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000412585.6:c.409_410insGCCTCCTCCGCGGGT ENSP00000399168.2:p.His137delinsArgLeuLeuArgGlyTyr
ENST00000434333.1:c.442_443insGCCTCCTCCGCGGGT ENSP00000405931.1:p.His148delinsArgLeuLeuArgGlyTyr
ENST00000474381.1:n.284_285insGCCTCCTCCGCGGGT
ENST00000498007.1:n.675_676insGCCTCCTCCGCGGGT
NM_005514.6:c.409_410insGCCTCCTCCGCGGGT NP_005505.2:p.His137delinsArgLeuLeuArgGlyTyr
XM_011514556.1:c.442_443insGCCTCCTCCGCGGGT XP_011512858.1:p.His148delinsArgLeuLeuArgGlyTyr
XM_011514557.1:c.409_410insGCCTCCTCCGCGGGT XP_011512859.1:p.His137delinsArgLeuLeuArgGlyTyr
XR_926175.1:n.419_420insGCCTCCTCCGCGGGT
NM_005514.7:c.409_410insGCCTCCTCCGCGGGT NP_005505.2:p.His137delinsArgLeuLeuArgGlyTyr
NM_005514.8:c.409_410insGCCTCCTCCGCGGGT MANE Select NP_005505.2:p.His137delinsArgLeuLeuArgGlyTyr
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