Canonical Allele Identifier: CA2677957594
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356688del , CM000668.2:g.31356688del GRCh38
NC_000006.11:g.31324465del , CM000668.1:g.31324465del GRCh37
NC_000006.10:g.31432444del NCBI36
NG_023187.1:g.5526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1816+1del
ENST00000481849.6:n.1816+1del
ENST00000497377.6:n.1816+1del
ENST00000640094.2:c.343+1del
ENST00000696558.1:c.343+1del
ENST00000696559.1:c.343+1del
ENST00000696560.1:c.343+1del
ENST00000696561.1:c.343+1del
ENST00000696562.1:c.343+1del
ENST00000412585.7:c.343+1del
ENST00000412585.6:c.343+1del
ENST00000434333.1:c.376+1del
ENST00000474381.1:n.218+1del
ENST00000498007.1:n.365del
ENST00000603274.1:n.42del
NM_005514.6:c.343+1del
XM_011514556.1:c.376+1del
XM_011514557.1:c.343+1del
XR_926175.1:n.353+1del
NM_005514.7:c.343+1del
NM_005514.8:c.343+1del