Canonical Allele Identifier: CA2677956543
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356150_31356174del , CM000668.2:g.31356150_31356174del GRCh38
NC_000006.11:g.31323927_31323951del , CM000668.1:g.31323927_31323951del GRCh37
NC_000006.10:g.31431906_31431930del NCBI36
NG_023187.1:g.6040_6064del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2086_2110del
ENST00000481849.6:n.2086_2092+18del
ENST00000497377.6:n.2086_2092+18del
ENST00000640094.2:c.613_619+18del
ENST00000696558.1:c.613_619+18del
ENST00000696559.1:c.613_619+18del
ENST00000696560.1:c.613_619+18del
ENST00000696561.1:c.613_619+18del
ENST00000696562.1:c.613_619+18del
ENST00000412585.7:c.613_619+18del
ENST00000412585.6:c.613_619+18del
ENST00000434333.1:c.646_652+18del
ENST00000474381.1:n.488_512del
ENST00000498007.1:n.879_885+18del
NM_005514.6:c.613_619+18del
XM_011514556.1:c.646_652+18del
XM_011514557.1:c.613_619+18del
XR_926175.1:n.623_647del
NM_005514.7:c.613_619+18del
NM_005514.8:c.613_619+18del