Canonical Allele Identifier: CA2677956092

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355983-CGTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355984_31355987del , CM000668.2:g.31355984_31355987del	GRCh38
NC_000006.11:g.31323761_31323764del , CM000668.1:g.31323761_31323764del	GRCh37
NC_000006.10:g.31431740_31431743del	NCBI36
NG_023187.1:g.6226_6229del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2272_2275del
ENST00000481849.6:n.2092+180_2092+183del
ENST00000497377.6:n.2092+180_2092+183del
ENST00000640094.2:c.619+180_619+183del	ENSP00000491275.2:n.619+180_619+183del
ENST00000696558.1:c.620-181_620-178del	ENSP00000512716.1:n.620-181_620-178del
ENST00000696559.1:c.619+180_619+183del	ENSP00000512717.1:n.619+180_619+183del
ENST00000696560.1:c.619+180_619+183del	ENSP00000512718.1:n.619+180_619+183del
ENST00000696561.1:c.619+180_619+183del	ENSP00000512719.1:n.619+180_619+183del
ENST00000696562.1:c.619+180_619+183del	ENSP00000512720.1:n.619+180_619+183del
ENST00000412585.7:c.619+180_619+183del MANE Select	ENSP00000399168.2:n.619+180_619+183del
ENST00000412585.6:c.619+180_619+183del	ENSP00000399168.2:n.619+180_619+183del
ENST00000434333.1:c.652+180_652+183del	ENSP00000405931.1:n.652+180_652+183del
ENST00000474381.1:n.674_677del
ENST00000498007.1:n.885+180_885+183del
NM_005514.6:c.619+180_619+183del	NP_005505.2:n.619+180_619+183del
XM_011514556.1:c.652+180_652+183del	XP_011512858.1:n.652+180_652+183del
XM_011514557.1:c.619+180_619+183del	XP_011512859.1:n.619+180_619+183del
XR_926175.1:n.809_812del
NM_005514.7:c.619+180_619+183del	NP_005505.2:n.619+180_619+183del
NM_005514.8:c.619+180_619+183del MANE Select	NP_005505.2:n.619+180_619+183del