Canonical Allele Identifier: CA2770503538

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354578_31354582dup , CM000668.2:g.31354578_31354582dup	GRCh38
NC_000006.11:g.31322355_31322359dup , CM000668.1:g.31322355_31322359dup	GRCh37
NC_000006.10:g.31430334_31430338dup	NCBI36
NG_023187.1:g.7634_7638dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3093-53_3093-49dup
ENST00000481849.6:n.3053-53_3053-49dup
ENST00000497377.6:n.2960-53_2960-49dup
ENST00000640094.2:c.929-53_929-49dup	ENSP00000491275.2:n.929-53_929-49dup
ENST00000696558.1:c.1115-53_1115-49dup	ENSP00000512716.1:n.1115-53_1115-49dup
ENST00000696559.1:c.1046-53_1046-49dup	ENSP00000512717.1:n.1046-53_1046-49dup
ENST00000696560.1:c.1046-53_1046-49dup	ENSP00000512718.1:n.1046-53_1046-49dup
ENST00000696561.1:c.1046-53_1046-49dup	ENSP00000512719.1:n.1046-53_1046-49dup
ENST00000696562.1:c.1046-53_1046-49dup	ENSP00000512720.1:n.1046-53_1046-49dup
ENST00000412585.7:c.1046-53_1046-49dup MANE Select	ENSP00000399168.2:n.1046-53_1046-49dup
ENST00000640094.1:c.122-53_122-49dup	ENSP00000491275.1:n.122-53_122-49dup
ENST00000412585.6:c.1046-53_1046-49dup	ENSP00000399168.2:n.1046-53_1046-49dup
ENST00000481849.5:n.228_232dup
ENST00000497377.5:n.445-53_445-49dup
NM_005514.6:c.1046-53_1046-49dup	NP_005505.2:n.1046-53_1046-49dup
XM_011514556.1:c.1079-53_1079-49dup	XP_011512858.1:n.1079-53_1079-49dup
XM_011514557.1:c.929-53_929-49dup	XP_011512859.1:n.929-53_929-49dup
XR_926175.1:n.1485-53_1485-49dup
NM_005514.7:c.1046-53_1046-49dup	NP_005505.2:n.1046-53_1046-49dup
NM_005514.8:c.1046-53_1046-49dup MANE Select	NP_005505.2:n.1046-53_1046-49dup