Canonical Allele Identifier: CA1619113858
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356973_31356983delinsGGCTGAGACCC , CM000668.2:g.31356973_31356983delinsGGCTGAGACCC GRCh38
NC_000006.11:g.31324750_31324760delinsGGCTGAGACCC , CM000668.1:g.31324750_31324760delinsGGCTGAGACCC GRCh37
NC_000006.10:g.31432729_31432739delinsGGCTGAGACCC NCBI36
NG_023187.1:g.5230_5240delinsGGGTCTCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1547-26_1547-16delinsGGGTCTCAGCC
ENST00000481849.6:n.1547-26_1547-16delinsGGGTCTCAGCC
ENST00000497377.6:n.1547-26_1547-16delinsGGGTCTCAGCC
ENST00000640094.2:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000491275.2:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000696558.1:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000512716.1:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000696559.1:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000512717.1:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000696560.1:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000512718.1:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000696561.1:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000512719.1:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000696562.1:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000512720.1:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000412585.7:c.74-26_74-16delinsGGGTCTCAGCC MANE Select ENSP00000399168.2:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000412585.6:c.74-26_74-16delinsGGGTCTCAGCC ENSP00000399168.2:n.74-26_74-16delinsGGGTCTCAGCC
ENST00000434333.1:c.81_91delinsGGGTCTCAGCC ENSP00000405931.1:p.Ala27=
ENST00000498007.1:n.95-26_95-16delinsGGGTCTCAGCC
ENST00000603274.1:n.327_337delinsGGCTGAGACCC
NM_005514.6:c.74-26_74-16delinsGGGTCTCAGCC NP_005505.2:n.74-26_74-16delinsGGGTCTCAGCC
XM_011514556.1:c.81_91delinsGGGTCTCAGCC XP_011512858.1:p.Ala27=
XM_011514557.1:c.74-26_74-16delinsGGGTCTCAGCC XP_011512859.1:n.74-26_74-16delinsGGGTCTCAGCC
XR_926175.1:n.84-26_84-16delinsGGGTCTCAGCC
NM_005514.7:c.74-26_74-16delinsGGGTCTCAGCC NP_005505.2:n.74-26_74-16delinsGGGTCTCAGCC
NM_005514.8:c.74-26_74-16delinsGGGTCTCAGCC MANE Select NP_005505.2:n.74-26_74-16delinsGGGTCTCAGCC