Canonical Allele Identifier: CA2677956490

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356128-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356131_31356132del , CM000668.2:g.31356131_31356132del	GRCh38
NC_000006.11:g.31323908_31323909del , CM000668.1:g.31323908_31323909del	GRCh37
NC_000006.10:g.31431887_31431888del	NCBI36
NG_023187.1:g.6083_6084del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2129_2130del
ENST00000481849.6:n.2092+37_2092+38del
ENST00000497377.6:n.2092+37_2092+38del
ENST00000640094.2:c.619+37_619+38del	ENSP00000491275.2:n.619+37_619+38del
ENST00000696558.1:c.619+37_619+38del	ENSP00000512716.1:n.619+37_619+38del
ENST00000696559.1:c.619+37_619+38del	ENSP00000512717.1:n.619+37_619+38del
ENST00000696560.1:c.619+37_619+38del	ENSP00000512718.1:n.619+37_619+38del
ENST00000696561.1:c.619+37_619+38del	ENSP00000512719.1:n.619+37_619+38del
ENST00000696562.1:c.619+37_619+38del	ENSP00000512720.1:n.619+37_619+38del
ENST00000412585.7:c.619+37_619+38del MANE Select	ENSP00000399168.2:n.619+37_619+38del
ENST00000412585.6:c.619+37_619+38del	ENSP00000399168.2:n.619+37_619+38del
ENST00000434333.1:c.652+37_652+38del	ENSP00000405931.1:n.652+37_652+38del
ENST00000474381.1:n.531_532del
ENST00000498007.1:n.885+37_885+38del
NM_005514.6:c.619+37_619+38del	NP_005505.2:n.619+37_619+38del
XM_011514556.1:c.652+37_652+38del	XP_011512858.1:n.652+37_652+38del
XM_011514557.1:c.619+37_619+38del	XP_011512859.1:n.619+37_619+38del
XR_926175.1:n.666_667del
NM_005514.7:c.619+37_619+38del	NP_005505.2:n.619+37_619+38del
NM_005514.8:c.619+37_619+38del MANE Select	NP_005505.2:n.619+37_619+38del