Canonical Allele Identifier: CA2677953099

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354141-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354143_31354144dup , CM000668.2:g.31354143_31354144dup	GRCh38
NC_000006.11:g.31321920_31321921dup , CM000668.1:g.31321920_31321921dup	GRCh37
NC_000006.10:g.31429899_31429900dup	NCBI36
NG_023187.1:g.8070_8071dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3294_3295dup
ENST00000481849.6:n.3254_3255dup
ENST00000497377.6:n.3161_3162dup
ENST00000696558.1:c.1316_1317dup	ENSP00000512716.1:n.1316_1317dup
ENST00000696559.1:c.*158_*159dup	ENSP00000512717.1:n.*158_*159dup
ENST00000696560.1:c.*158_*159dup	ENSP00000512718.1:n.*158_*159dup
ENST00000696561.1:c.*158_*159dup	ENSP00000512719.1:n.*158_*159dup
ENST00000696562.1:c.*158_*159dup	ENSP00000512720.1:n.*158_*159dup
ENST00000412585.7:c.*158_*159dup MANE Select	ENSP00000399168.2:n.*158_*159dup
ENST00000412585.6:c.*158_*159dup	ENSP00000399168.2:n.*158_*159dup
ENST00000481849.5:n.482_483dup
ENST00000497377.5:n.646_647dup
NM_005514.6:c.*158_*159dup	NP_005505.2:n.*158_*159dup
XM_011514556.1:c.*158_*159dup	XP_011512858.1:n.*158_*159dup
XM_011514557.1:c.*158_*159dup	XP_011512859.1:n.*158_*159dup
XR_926175.1:n.1686_1687dup
NM_005514.7:c.*158_*159dup	NP_005505.2:n.*158_*159dup
NM_005514.8:c.*158_*159dup MANE Select	NP_005505.2:n.*158_*159dup