Canonical Allele Identifier: CA1619113786

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356958_31356959delinsCT , CM000668.2:g.31356958_31356959delinsCT	GRCh38
NC_000006.11:g.31324735_31324736delinsCT , CM000668.1:g.31324735_31324736delinsCT	GRCh37
NC_000006.10:g.31432714_31432715delinsCT	NCBI36
NG_023187.1:g.5254_5255delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1547-2_1547-1delinsAG
ENST00000481849.6:n.1547-2_1547-1delinsAG
ENST00000497377.6:n.1547-2_1547-1delinsAG
ENST00000640094.2:c.74-2_74-1delinsAG	ENSP00000491275.2:n.74-2_74-1delinsAG
ENST00000696558.1:c.74-2_74-1delinsAG	ENSP00000512716.1:n.74-2_74-1delinsAG
ENST00000696559.1:c.74-2_74-1delinsAG	ENSP00000512717.1:n.74-2_74-1delinsAG
ENST00000696560.1:c.74-2_74-1delinsAG	ENSP00000512718.1:n.74-2_74-1delinsAG
ENST00000696561.1:c.74-2_74-1delinsAG	ENSP00000512719.1:n.74-2_74-1delinsAG
ENST00000696562.1:c.74-2_74-1delinsAG	ENSP00000512720.1:n.74-2_74-1delinsAG
ENST00000412585.7:c.74-2_74-1delinsAG MANE Select	ENSP00000399168.2:n.74-2_74-1delinsAG
ENST00000412585.6:c.74-2_74-1delinsAG	ENSP00000399168.2:n.74-2_74-1delinsAG
ENST00000434333.1:c.105_106delinsAG	ENSP00000405931.1:p.Pro35=
ENST00000498007.1:n.95-2_95-1delinsAG
ENST00000603274.1:n.312_313delinsCT
NM_005514.6:c.74-2_74-1delinsAG	NP_005505.2:n.74-2_74-1delinsAG
XM_011514556.1:c.105_106delinsAG	XP_011512858.1:p.Pro35=
XM_011514557.1:c.74-2_74-1delinsAG	XP_011512859.1:n.74-2_74-1delinsAG
XR_926175.1:n.84-2_84-1delinsAG
NM_005514.7:c.74-2_74-1delinsAG	NP_005505.2:n.74-2_74-1delinsAG
NM_005514.8:c.74-2_74-1delinsAG MANE Select	NP_005505.2:n.74-2_74-1delinsAG