Canonical Allele Identifier: CA1087469099
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v3: 6-31356668-CCCGGGCCGGGGTCACTCACCGGCCTCGCTCTGGTTGTAGTAGCCGCGCAGGTTCCGCAGGCTCTCTCGGTCAGTCTGTGCCTGGGCCTTGTAGATCTGTGTGTTCCGGTCCCAATACTCCGGCCCCTCCTGCTCTATCCACGGCGCCCGCGGCTCCTCTCTCGGACTCGCGGCGTCGCTGTCGAACCTCACGAACTGGGTGTCGTCCACGTAGCCCACTGAGATGAAGCGGGGCTCCCCGCGG-C
gnomAD v4: 6-31356668-CCCGGGCCGGGGTCACTCACCGGCCTCGCTCTGGTTGTAGTAGCCGCGCAGGTTCCGCAGGCTCTCTCGGTCAGTCTGTGCCTGGGCCTTGTAGATCTGTGTGTTCCGGTCCCAATACTCCGGCCCCTCCTGCTCTATCCACGGCGCCCGCGGCTCCTCTCTCGGACTCGCGGCGTCGCTGTCGAACCTCACGAACTGGGTGTCGTCCACGTAGCCCACTGAGATGAAGCGGGGCTCCCCGCGG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356679_31356921del , CM000668.2:g.31356679_31356921del GRCh38
NC_000006.11:g.31324456_31324698del , CM000668.1:g.31324456_31324698del GRCh37
NC_000006.10:g.31432435_31432677del NCBI36
NG_023187.1:g.5302_5544del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1593_1816+19del
ENST00000481849.6:n.1593_1816+19del
ENST00000497377.6:n.1593_1816+19del
ENST00000640094.2:c.120_343+19del
ENST00000696558.1:c.120_343+19del
ENST00000696559.1:c.120_343+19del
ENST00000696560.1:c.120_343+19del
ENST00000696561.1:c.120_343+19del
ENST00000696562.1:c.120_343+19del
ENST00000412585.7:c.120_343+19del
ENST00000412585.6:c.120_343+19del
ENST00000434333.1:c.153_376+19del
ENST00000498007.1:n.141_383del
ENST00000603274.1:n.33_275del
NM_005514.6:c.120_343+19del
XM_011514556.1:c.153_376+19del
XM_011514557.1:c.120_343+19del
XR_926175.1:n.130_353+19del
NM_005514.7:c.120_343+19del
NM_005514.8:c.120_343+19del
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