Canonical Allele Identifier: CA2677954323

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354590-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354594dup , CM000668.2:g.31354594dup	GRCh38
NC_000006.11:g.31322371dup , CM000668.1:g.31322371dup	GRCh37
NC_000006.10:g.31430350dup	NCBI36
NG_023187.1:g.7622dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+42dup
ENST00000481849.6:n.3052+42dup
ENST00000497377.6:n.2959+42dup
ENST00000640094.2:c.928+42dup	ENSP00000491275.2:n.928+42dup
ENST00000696558.1:c.1114+42dup	ENSP00000512716.1:n.1114+42dup
ENST00000696559.1:c.1045+42dup	ENSP00000512717.1:n.1045+42dup
ENST00000696560.1:c.1045+42dup	ENSP00000512718.1:n.1045+42dup
ENST00000696561.1:c.1045+42dup	ENSP00000512719.1:n.1045+42dup
ENST00000696562.1:c.1045+42dup	ENSP00000512720.1:n.1045+42dup
ENST00000412585.7:c.1045+42dup MANE Select	ENSP00000399168.2:n.1045+42dup
ENST00000640094.1:c.121+42dup	ENSP00000491275.1:n.121+42dup
ENST00000412585.6:c.1045+42dup	ENSP00000399168.2:n.1045+42dup
ENST00000481849.5:n.216dup
ENST00000497377.5:n.444+42dup
NM_005514.6:c.1045+42dup	NP_005505.2:n.1045+42dup
XM_011514556.1:c.1078+42dup	XP_011512858.1:n.1078+42dup
XM_011514557.1:c.928+42dup	XP_011512859.1:n.928+42dup
XR_926175.1:n.1484+42dup
NM_005514.7:c.1045+42dup	NP_005505.2:n.1045+42dup
NM_005514.8:c.1045+42dup MANE Select	NP_005505.2:n.1045+42dup