Canonical Allele Identifier: CA1619118283

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766806511

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355159_31355160insGCTACGGTG , CM000668.2:g.31355159_31355160insGCTACGGTG	GRCh38
NC_000006.11:g.31322936_31322937insGCTACGGTG , CM000668.1:g.31322936_31322937insGCTACGGTG	GRCh37
NC_000006.10:g.31430915_31430916insGCTACGGTG	NCBI36
NG_023187.1:g.7053_7054insCACCGTAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3006_3007insCACCGTAGC
ENST00000481849.6:n.2525_2526insCACCGTAGC
ENST00000497377.6:n.2432_2433insCACCGTAGC
ENST00000640094.2:c.895+157_895+158insCACCGTAGC	ENSP00000491275.2:n.895+157_895+158insCACCGTAGC
ENST00000696558.1:c.1028_1029insCACCGTAGC	ENSP00000512716.1:n.1028_1029insCACCGTAGC
ENST00000696559.1:c.959_960insCACCGTAGC	ENSP00000512717.1:p.Val320_Val321insThrValAla
ENST00000696560.1:c.959_960insCACCGTAGC	ENSP00000512718.1:p.Val320_Val321insThrValAla
ENST00000696561.1:c.959_960insCACCGTAGC	ENSP00000512719.1:p.Val320_Val321insThrValAla
ENST00000696562.1:c.959_960insCACCGTAGC	ENSP00000512720.1:p.Val320_Val321insThrValAla
ENST00000412585.7:c.959_960insCACCGTAGC MANE Select	ENSP00000399168.2:p.Val320_Val321insThrValAla
ENST00000640094.1:c.88+157_88+158insCACCGTAGC	ENSP00000491275.1:n.88+157_88+158insCACCGTAGC
ENST00000412585.6:c.959_960insCACCGTAGC	ENSP00000399168.2:p.Val320_Val321insThrValAla
ENST00000463574.1:n.550_551insCACCGTAGC
NM_005514.6:c.959_960insCACCGTAGC	NP_005505.2:p.Val320_Val321insThrValAla
XM_011514556.1:c.992_993insCACCGTAGC	XP_011512858.1:p.Val331_Val332insThrValAla
XM_011514557.1:c.895+157_895+158insCACCGTAGC	XP_011512859.1:n.895+157_895+158insCACCGTAGC
XR_926175.1:n.1398_1399insCACCGTAGC
NM_005514.7:c.959_960insCACCGTAGC	NP_005505.2:p.Val320_Val321insThrValAla
NM_005514.8:c.959_960insCACCGTAGC MANE Select	NP_005505.2:p.Val320_Val321insThrValAla