Canonical Allele Identifier: CA2677954490

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354808-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354809_31354810del , CM000668.2:g.31354809_31354810del	GRCh38
NC_000006.11:g.31322586_31322587del , CM000668.1:g.31322586_31322587del	GRCh37
NC_000006.10:g.31430565_31430566del	NCBI36
NG_023187.1:g.7403_7404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3060-145_3060-144del
ENST00000481849.6:n.2875_2876del
ENST00000497377.6:n.2782_2783del
ENST00000640094.2:c.896-145_896-144del	ENSP00000491275.2:n.896-145_896-144del
ENST00000696558.1:c.1082-145_1082-144del	ENSP00000512716.1:n.1082-145_1082-144del
ENST00000696559.1:c.1013-145_1013-144del	ENSP00000512717.1:n.1013-145_1013-144del
ENST00000696560.1:c.1013-145_1013-144del	ENSP00000512718.1:n.1013-145_1013-144del
ENST00000696561.1:c.1013-145_1013-144del	ENSP00000512719.1:n.1013-145_1013-144del
ENST00000696562.1:c.1013-145_1013-144del	ENSP00000512720.1:n.1013-145_1013-144del
ENST00000412585.7:c.1013-145_1013-144del MANE Select	ENSP00000399168.2:n.1013-145_1013-144del
ENST00000640094.1:c.89-145_89-144del	ENSP00000491275.1:n.89-145_89-144del
ENST00000412585.6:c.1013-145_1013-144del	ENSP00000399168.2:n.1013-145_1013-144del
ENST00000497377.5:n.267_268del
NM_005514.6:c.1013-145_1013-144del	NP_005505.2:n.1013-145_1013-144del
XM_011514556.1:c.1046-145_1046-144del	XP_011512858.1:n.1046-145_1046-144del
XM_011514557.1:c.896-145_896-144del	XP_011512859.1:n.896-145_896-144del
XR_926175.1:n.1452-145_1452-144del
NM_005514.7:c.1013-145_1013-144del	NP_005505.2:n.1013-145_1013-144del
NM_005514.8:c.1013-145_1013-144del MANE Select	NP_005505.2:n.1013-145_1013-144del