Canonical Allele Identifier: CA2677956988
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356444_31356475del , CM000668.2:g.31356444_31356475del GRCh38
NC_000006.11:g.31324221_31324252del , CM000668.1:g.31324221_31324252del GRCh37
NC_000006.10:g.31432200_31432231del NCBI36
NG_023187.1:g.5741_5772del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-30_1818del
ENST00000481849.6:n.1817-30_1818del
ENST00000497377.6:n.1817-30_1818del
ENST00000640094.2:c.344-30_345del
ENST00000696558.1:c.344-30_345del
ENST00000696559.1:c.344-30_345del
ENST00000696560.1:c.344-30_345del
ENST00000696561.1:c.344-30_345del
ENST00000696562.1:c.344-30_345del
ENST00000412585.7:c.344-30_345del
ENST00000412585.6:c.344-30_345del
ENST00000434333.1:c.377-30_378del
ENST00000474381.1:n.219-30_220del
ENST00000498007.1:n.580_611del
NM_005514.6:c.344-30_345del
XM_011514556.1:c.377-30_378del
XM_011514557.1:c.344-30_345del
XR_926175.1:n.354-30_355del
NM_005514.7:c.344-30_345del
NM_005514.8:c.344-30_345del