Canonical Allele Identifier: CA2594586122
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs2113743946

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356290_31356292dup , CM000668.2:g.31356290_31356292dup GRCh38
NC_000006.11:g.31324067_31324069dup , CM000668.1:g.31324067_31324069dup GRCh37
NC_000006.10:g.31432046_31432048dup NCBI36
NG_023187.1:g.5921_5923dup

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1967_1969dup
ENST00000481849.6:n.1967_1969dup
ENST00000497377.6:n.1967_1969dup
ENST00000640094.2:c.494_496dup ENSP00000491275.2:p.Gln165_Ile166insLys
ENST00000696558.1:c.494_496dup ENSP00000512716.1:p.Gln165_Ile166insLys
ENST00000696559.1:c.494_496dup ENSP00000512717.1:p.Gln165_Ile166insLys
ENST00000696560.1:c.494_496dup ENSP00000512718.1:p.Gln165_Ile166insLys
ENST00000696561.1:c.494_496dup ENSP00000512719.1:p.Gln165_Ile166insLys
ENST00000696562.1:c.494_496dup ENSP00000512720.1:p.Gln165_Ile166insLys
ENST00000412585.7:c.494_496dup MANE Select ENSP00000399168.2:p.Gln165_Ile166insLys
ENST00000412585.6:c.494_496dup ENSP00000399168.2:p.Gln165_Ile166insLys
ENST00000434333.1:c.527_529dup ENSP00000405931.1:p.Gln176_Ile177insLys
ENST00000474381.1:n.369_371dup
ENST00000498007.1:n.760_762dup
NM_005514.6:c.494_496dup NP_005505.2:p.Gln165_Ile166insLys
XM_011514556.1:c.527_529dup XP_011512858.1:p.Gln176_Ile177insLys
XM_011514557.1:c.494_496dup XP_011512859.1:p.Gln165_Ile166insLys
XR_926175.1:n.504_506dup
NM_005514.7:c.494_496dup NP_005505.2:p.Gln165_Ile166insLys
NM_005514.8:c.494_496dup MANE Select NP_005505.2:p.Gln165_Ile166insLys