Canonical Allele Identifier: CA2677955547
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31355767-TCGA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355768_31355770del , CM000668.2:g.31355768_31355770del GRCh38
NC_000006.11:g.31323545_31323547del , CM000668.1:g.31323545_31323547del GRCh37
NC_000006.10:g.31431524_31431526del NCBI36
NG_023187.1:g.6443_6445del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2489_2491del
ENST00000481849.6:n.2093-178_2093-176del
ENST00000497377.6:n.2093-178_2093-176del
ENST00000640094.2:c.620-178_620-176del ENSP00000491275.2:n.620-178_620-176del
ENST00000696558.1:c.656_658del ENSP00000512716.1:p.Leu219_Glu220delinsGl...
ENST00000696559.1:c.620-178_620-176del ENSP00000512717.1:n.620-178_620-176del
ENST00000696560.1:c.620-178_620-176del ENSP00000512718.1:n.620-178_620-176del
ENST00000696561.1:c.620-178_620-176del ENSP00000512719.1:n.620-178_620-176del
ENST00000696562.1:c.620-178_620-176del ENSP00000512720.1:n.620-178_620-176del
ENST00000412585.7:c.620-178_620-176del MANE Select ENSP00000399168.2:n.620-178_620-176del
ENST00000412585.6:c.620-178_620-176del ENSP00000399168.2:n.620-178_620-176del
ENST00000434333.1:c.653-178_653-176del ENSP00000405931.1:n.653-178_653-176del
ENST00000463574.1:n.33_35del
ENST00000474381.1:n.891_893del
ENST00000498007.1:n.886-178_886-176del
NM_005514.6:c.620-178_620-176del NP_005505.2:n.620-178_620-176del
XM_011514556.1:c.653-178_653-176del XP_011512858.1:n.653-178_653-176del
XM_011514557.1:c.620-178_620-176del XP_011512859.1:n.620-178_620-176del
XR_926175.1:n.1026_1028del
NM_005514.7:c.620-178_620-176del NP_005505.2:n.620-178_620-176del
NM_005514.8:c.620-178_620-176del MANE Select NP_005505.2:n.620-178_620-176del
Search 100 bp 5'
Search 100 bp 3'