Canonical Allele Identifier: CA3711082
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs71920763
ExAC: 6:31322209 AC / A
gnomAD v2: 6-31322209-AC-A
gnomAD v4: 6-31354432-AC-A
MyVariant Identifiers: chr6:g.31322210del (hg19) chr6:g.31322214_31322218delinsAGAC (hg19) chr6:g.31354433del (hg38) chr6:g.31354437_31354441delinsAGAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354437del , CM000668.2:g.31354437del GRCh38
NC_000006.11:g.31322214del , CM000668.1:g.31322214del GRCh37
NC_000006.10:g.31430193del NCBI36
NG_023187.1:g.7780del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3140+46del
ENST00000481849.6:n.3100+46del
ENST00000497377.6:n.3007+46del
ENST00000696558.1:c.1162+46del ENSP00000512716.1:n.1162+46del
ENST00000696559.1:c.*4+46del ENSP00000512717.1:n.*4+46del
ENST00000696560.1:c.*4+46del ENSP00000512718.1:n.*4+46del
ENST00000696561.1:c.*4+46del ENSP00000512719.1:n.*4+46del
ENST00000696562.1:c.*4+46del ENSP00000512720.1:n.*4+46del
ENST00000412585.7:c.*4+46del MANE Select ENSP00000399168.2:n.*4+46del
ENST00000412585.6:c.*4+46del ENSP00000399168.2:n.*4+46del
ENST00000481849.5:n.328+46del
ENST00000497377.5:n.492+46del
NM_005514.6:c.*4+46del NP_005505.2:n.*4+46del
XM_011514556.1:c.*4+46del XP_011512858.1:n.*4+46del
XM_011514557.1:c.*4+46del XP_011512859.1:n.*4+46del
XR_926175.1:n.1532+46del
NM_005514.7:c.*4+46del NP_005505.2:n.*4+46del
NM_005514.8:c.*4+46del MANE Select NP_005505.2:n.*4+46del
Search 100 bp 5'
Search 100 bp 3'