Canonical Allele Identifier: CA2677954301

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354575-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354576_31354577del , CM000668.2:g.31354576_31354577del	GRCh38
NC_000006.11:g.31322353_31322354del , CM000668.1:g.31322353_31322354del	GRCh37
NC_000006.10:g.31430332_31430333del	NCBI36
NG_023187.1:g.7636_7637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3093-51_3093-50del
ENST00000481849.6:n.3053-51_3053-50del
ENST00000497377.6:n.2960-51_2960-50del
ENST00000640094.2:c.929-51_929-50del	ENSP00000491275.2:n.929-51_929-50del
ENST00000696558.1:c.1115-51_1115-50del	ENSP00000512716.1:n.1115-51_1115-50del
ENST00000696559.1:c.1046-51_1046-50del	ENSP00000512717.1:n.1046-51_1046-50del
ENST00000696560.1:c.1046-51_1046-50del	ENSP00000512718.1:n.1046-51_1046-50del
ENST00000696561.1:c.1046-51_1046-50del	ENSP00000512719.1:n.1046-51_1046-50del
ENST00000696562.1:c.1046-51_1046-50del	ENSP00000512720.1:n.1046-51_1046-50del
ENST00000412585.7:c.1046-51_1046-50del MANE Select	ENSP00000399168.2:n.1046-51_1046-50del
ENST00000640094.1:c.122-51_122-50del	ENSP00000491275.1:n.122-51_122-50del
ENST00000412585.6:c.1046-51_1046-50del	ENSP00000399168.2:n.1046-51_1046-50del
ENST00000481849.5:n.230_231del
ENST00000497377.5:n.445-51_445-50del
NM_005514.6:c.1046-51_1046-50del	NP_005505.2:n.1046-51_1046-50del
XM_011514556.1:c.1079-51_1079-50del	XP_011512858.1:n.1079-51_1079-50del
XM_011514557.1:c.929-51_929-50del	XP_011512859.1:n.929-51_929-50del
XR_926175.1:n.1485-51_1485-50del
NM_005514.7:c.1046-51_1046-50del	NP_005505.2:n.1046-51_1046-50del
NM_005514.8:c.1046-51_1046-50del MANE Select	NP_005505.2:n.1046-51_1046-50del