Canonical Allele Identifier: CA2677957320
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31356489-C-CCCGGTCCCCCGAGCCCCGCCCCAGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356491_31356492insGGTCCCCCGAGCCCCGCCCCAGTCC , CM000668.2:g.31356491_31356492insGGTCCCCCGAGCCCCGCCCCAGTCC GRCh38
NC_000006.11:g.31324268_31324269insGGTCCCCCGAGCCCCGCCCCAGTCC , CM000668.1:g.31324268_31324269insGGTCCCCCGAGCCCCGCCCCAGTCC GRCh37
NC_000006.10:g.31432247_31432248insGGTCCCCCGAGCCCCGCCCCAGTCC NCBI36
NG_023187.1:g.5723_5724insACTGGGGCGGGGCTCGGGGGACCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-48_1817-47insACTGGGGCGGGGCTCGGGGGACCGG
ENST00000481849.6:n.1817-48_1817-47insACTGGGGCGGGGCTCGGGGGACCGG
ENST00000497377.6:n.1817-48_1817-47insACTGGGGCGGGGCTCGGGGGACCGG
ENST00000640094.2:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000491275.2:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000696558.1:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000512716.1:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000696559.1:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000512717.1:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000696560.1:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000512718.1:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000696561.1:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000512719.1:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000696562.1:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000512720.1:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000412585.7:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG MANE Select ENSP00000399168.2:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000412585.6:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000399168.2:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000434333.1:c.377-48_377-47insACTGGGGCGGGGCTCGGGGGACCGG ENSP00000405931.1:n.377-48_377-47insACTGGGGCGGGGCTCGGGGGACCGG...
ENST00000474381.1:n.219-48_219-47insACTGGGGCGGGGCTCGGGGGACCGG
ENST00000498007.1:n.562_563insACTGGGGCGGGGCTCGGGGGACCGG
NM_005514.6:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG NP_005505.2:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG
XM_011514556.1:c.377-48_377-47insACTGGGGCGGGGCTCGGGGGACCGG XP_011512858.1:n.377-48_377-47insACTGGGGCGGGGCTCGGGGGACCGG
XM_011514557.1:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG XP_011512859.1:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG
XR_926175.1:n.354-48_354-47insACTGGGGCGGGGCTCGGGGGACCGG
NM_005514.7:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG NP_005505.2:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG
NM_005514.8:c.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG MANE Select NP_005505.2:n.344-48_344-47insACTGGGGCGGGGCTCGGGGGACCGG
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