Canonical Allele Identifier: CA2840254784
Gene: HLA-B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354427_31354428insCCCCCCCCCCCCACCCCCCCCCCCCCCCC , CM000668.2:g.31354427_31354428insCCCCCCCCCCCCACCCCCCCCCCCCCCCC GRCh38
NC_000006.11:g.31322204_31322205insCCCCCCCCCCCCACCCCCCCCCCCCCCCC , CM000668.1:g.31322204_31322205insCCCCCCCCCCCCACCCCCCCCCCCCCCCC GRCh37
NC_000006.10:g.31430183_31430184insCCCCCCCCCCCCACCCCCCCCCCCCCCCC NCBI36
NG_023187.1:g.7789_7790insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3140+55_3140+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
ENST00000481849.6:n.3100+55_3100+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
ENST00000497377.6:n.3007+55_3007+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
ENST00000696558.1:c.1162+55_1162+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG ENSP00000512716.1:n.1162+55_1162+56insGGGGGGGGGGGGTGGGGGGGGGG...
ENST00000696559.1:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG ENSP00000512717.1:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGG...
ENST00000696560.1:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG ENSP00000512718.1:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGG...
ENST00000696561.1:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG ENSP00000512719.1:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGG...
ENST00000696562.1:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG ENSP00000512720.1:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGG...
ENST00000412585.7:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG MANE Select ENSP00000399168.2:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGG...
ENST00000412585.6:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG ENSP00000399168.2:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGG...
ENST00000481849.5:n.328+55_328+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
ENST00000497377.5:n.492+55_492+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
NM_005514.6:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG NP_005505.2:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
XM_011514556.1:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG XP_011512858.1:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
XM_011514557.1:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG XP_011512859.1:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
XR_926175.1:n.1532+55_1532+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
NM_005514.7:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG NP_005505.2:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
NM_005514.8:c.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG MANE Select NP_005505.2:n.*4+55_*4+56insGGGGGGGGGGGGTGGGGGGGGGGGGGGGG
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