Canonical Allele Identifier: CA136836749
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341074
MyVariant Identifiers: chr6:g.31324931del (hg19) chr6:g.31357154del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357154del , CM000668.2:g.31357154del GRCh38
NC_000006.11:g.31324931del , CM000668.1:g.31324931del GRCh37
NC_000006.10:g.31432910del NCBI36
NG_023187.1:g.5059del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1478del
ENST00000481849.6:n.1478del
ENST00000497377.6:n.1478del
ENST00000640094.2:c.5del ENSP00000491275.2:p.Leu2ArgfsTer18
ENST00000696558.1:c.5del ENSP00000512716.1:p.Leu2ArgfsTer18
ENST00000696559.1:c.5del ENSP00000512717.1:p.Leu2ArgfsTer18
ENST00000696560.1:c.5del ENSP00000512718.1:p.Leu2ArgfsTer18
ENST00000696561.1:c.5del ENSP00000512719.1:p.Leu2ArgfsTer18
ENST00000696562.1:c.5del ENSP00000512720.1:p.Leu2ArgfsTer18
ENST00000412585.7:c.5del MANE Select ENSP00000399168.2:p.Leu2ArgfsTer18
ENST00000412585.6:c.5del ENSP00000399168.2:p.Leu2ArgfsTer18
ENST00000434333.1:c.-91del ENSP00000405931.1:n.-91del
ENST00000498007.1:n.26del
ENST00000603274.1:n.508del
NM_005514.6:c.5del NP_005505.2:p.Leu2ArgfsTer18
XM_011514557.1:c.5del XP_011512859.1:p.Leu2ArgfsTer18
XR_926175.1:n.15del
NM_005514.7:c.5del NP_005505.2:p.Leu2ArgfsTer18
NM_005514.8:c.5del MANE Select NP_005505.2:p.Leu2ArgfsTer18
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