Canonical Allele Identifier: CA1087464365
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v3: 6-31355086-CACCCCTCACCCCTTCCCTACCTGAACTCTTCCTCCTACACATCACAGCAGCGACCACAGCTCCGATGACCACAACTGCTAGGACAGCCAGGCCAGCAACAATGCCCACGATGGGGACGGTGGACTGGGAAGACGGCTCTGGGAAAGGAGGGGAAGATGAGGGGCCCTGACCCTGCTGAAGGGCTCCTGCTTTCCCTGAGAAGAGATATG-C
gnomAD v4: 6-31355086-CACCCCTCACCCCTTCCCTACCTGAACTCTTCCTCCTACACATCACAGCAGCGACCACAGCTCCGATGACCACAACTGCTAGGACAGCCAGGCCAGCAACAATGCCCACGATGGGGACGGTGGACTGGGAAGACGGCTCTGGGAAAGGAGGGGAAGATGAGGGGCCCTGACCCTGCTGAAGGGCTCCTGCTTTCCCTGAGAAGAGATATG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355095_31355303del , CM000668.2:g.31355095_31355303del GRCh38
NC_000006.11:g.31322872_31323080del , CM000668.1:g.31322872_31323080del GRCh37
NC_000006.10:g.31430851_31431059del NCBI36
NG_023187.1:g.6918_7126del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2942+22_3059+20del
ENST00000481849.6:n.2390_2598del
ENST00000497377.6:n.2368+22_2505del
ENST00000640094.2:c.895+22_895+230del ENSP00000491275.2:n.895+22_895+230del
ENST00000696558.1:c.964+22_1081+20del
ENST00000696559.1:c.895+22_1012+20del
ENST00000696560.1:c.895+22_1012+20del
ENST00000696561.1:c.895+22_1012+20del
ENST00000696562.1:c.895+22_1012+20del
ENST00000412585.7:c.895+22_1012+20del
ENST00000640094.1:c.88+22_88+230del ENSP00000491275.1:n.88+22_88+230del
ENST00000412585.6:c.895+22_1012+20del
NM_005514.6:c.895+22_1012+20del
XM_011514556.1:c.928+22_1045+20del
XM_011514557.1:c.895+22_895+230del XP_011512859.1:n.895+22_895+230del
XR_926175.1:n.1334+22_1451+20del
NM_005514.7:c.895+22_1012+20del
NM_005514.8:c.895+22_1012+20del
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