Canonical Allele Identifier: CA3711287
Gene: HLA-B HGNC NCBI

Linked Data

ExAC: 6:31323000 TCTGGGAAAGGAGGGGAAGATGAGGGGCCCTGACCCTGCTGAAGGGCTCCTGCTTTCCCTGAGAAGAGATATGACCCCTCATCCCCCTCCTTAC / T
gnomAD v2: 6-31323000-TCTGGGAAAGGAGGGGAAGATGAGGGGCCCTGACCCTGCTGAAGGGCTCCTGCTTTCCCTGAGAAGAGATATGACCCCTCATCCCCCTCCTTAC-T
gnomAD v4: 6-31355223-TCTGGGAAAGGAGGGGAAGATGAGGGGCCCTGACCCTGCTGAAGGGCTCCTGCTTTCCCTGAGAAGAGATATGACCCCTCATCCCCCTCCTTAC-T
MyVariant Identifiers: chr6:g.31323001_31323093del (hg19) chr6:g.31355224_31355316del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355225_31355317del , CM000668.2:g.31355225_31355317del GRCh38
NC_000006.11:g.31323002_31323094del , CM000668.1:g.31323002_31323094del GRCh37
NC_000006.10:g.31430981_31431073del NCBI36
NG_023187.1:g.6897_6989del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2942+1_2943-1del
ENST00000481849.6:n.2369_2461del
ENST00000497377.6:n.2368+1_2369-1del
ENST00000640094.2:c.895+1_895+93del
ENST00000696558.1:c.964+1_965-1del
ENST00000696559.1:c.895+1_896-1del
ENST00000696560.1:c.895+1_896-1del
ENST00000696561.1:c.895+1_896-1del
ENST00000696562.1:c.895+1_896-1del
ENST00000412585.7:c.895+1_896-1del
ENST00000640094.1:c.88+1_88+93del
ENST00000412585.6:c.895+1_896-1del
ENST00000463574.1:n.486+1_487-1del
NM_005514.6:c.895+1_896-1del
XM_011514556.1:c.928+1_929-1del
XM_011514557.1:c.895+1_895+93del
XR_926175.1:n.1334+1_1335-1del
NM_005514.7:c.895+1_896-1del
NM_005514.8:c.895+1_896-1del
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