Canonical Allele Identifier: CA2677957694

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356754-C-CTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356754_31356755insTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT , CM000668.2:g.31356754_31356755insTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT	GRCh38
NC_000006.11:g.31324531_31324532insTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT , CM000668.1:g.31324531_31324532insTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT	GRCh37
NC_000006.10:g.31432510_31432511insTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT	NCBI36
NG_023187.1:g.5458_5459insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1749_1750insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA
ENST00000481849.6:n.1749_1750insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA
ENST00000497377.6:n.1749_1750insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA
ENST00000640094.2:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000491275.2:p.Ala93ThrfsTer23
ENST00000696558.1:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000512716.1:p.Ala93ThrfsTer23
ENST00000696559.1:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000512717.1:p.Ala93ThrfsTer23
ENST00000696560.1:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000512718.1:p.Ala93ThrfsTer23
ENST00000696561.1:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000512719.1:p.Ala93ThrfsTer23
ENST00000696562.1:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000512720.1:p.Ala93ThrfsTer23
ENST00000412585.7:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA MANE Select	ENSP00000399168.2:p.Ala93ThrfsTer23
ENST00000412585.6:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000399168.2:p.Ala93ThrfsTer23
ENST00000434333.1:c.309_310insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	ENSP00000405931.1:p.Ala104ThrfsTer23
ENST00000474381.1:n.151_152insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA
ENST00000498007.1:n.297_298insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA
ENST00000603274.1:n.108_109insTCCTCCTGCTCCATCCACGGCGCCCGCGGCTCCGGTAAGTCTGTGTGTTGGT
NM_005514.6:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	NP_005505.2:p.Ala93ThrfsTer23
XM_011514556.1:c.309_310insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	XP_011512858.1:p.Ala104ThrfsTer23
XM_011514557.1:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	XP_011512859.1:p.Ala93ThrfsTer23
XR_926175.1:n.286_287insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA
NM_005514.7:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA	NP_005505.2:p.Ala93ThrfsTer23
NM_005514.8:c.276_277insACCAACACACAGACTTACCGGAGCCGCGGGCGCCGTGGATGGAGCAGGAGGA MANE Select	NP_005505.2:p.Ala93ThrfsTer23