Canonical Allele Identifier: CA566689268
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1156752221
gnomAD v2: 6-31325022-ATATC-A
gnomAD v3: 6-31357245-ATATC-A
gnomAD v4: 6-31357245-ATATC-A
MyVariant Identifiers: chr6:g.31325023_31325026del (hg19) chr6:g.31357246_31357249del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357246_31357249del , CM000668.2:g.31357246_31357249del GRCh38
NC_000006.11:g.31325023_31325026del , CM000668.1:g.31325023_31325026del GRCh37
NC_000006.10:g.31433002_31433005del NCBI36
NG_023187.1:g.4964_4967del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1383_1386del
ENST00000481849.6:n.1383_1386del
ENST00000497377.6:n.1383_1386del
ENST00000696559.1:c.-91_-88del ENSP00000512717.1:n.-91_-88del
ENST00000696560.1:c.-91_-88del ENSP00000512718.1:n.-91_-88del
ENST00000696561.1:c.-91_-88del ENSP00000512719.1:n.-91_-88del
ENST00000696562.1:c.-91_-88del ENSP00000512720.1:n.-91_-88del
ENST00000603274.1:n.600_603del
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