Canonical Allele Identifier: CA2677953000

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354088-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354089dup , CM000668.2:g.31354089dup	GRCh38
NC_000006.11:g.31321866dup , CM000668.1:g.31321866dup	GRCh37
NC_000006.10:g.31429845dup	NCBI36
NG_023187.1:g.8124dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3348dup
ENST00000481849.6:n.3308dup
ENST00000497377.6:n.3215dup
ENST00000696558.1:c.1370dup	ENSP00000512716.1:n.1370dup
ENST00000696559.1:c.*212dup	ENSP00000512717.1:n.*212dup
ENST00000696560.1:c.*212dup	ENSP00000512718.1:n.*212dup
ENST00000696561.1:c.*212dup	ENSP00000512719.1:n.*212dup
ENST00000696562.1:c.*212dup	ENSP00000512720.1:n.*212dup
ENST00000412585.7:c.*212dup MANE Select	ENSP00000399168.2:n.*212dup
ENST00000412585.6:c.*212dup	ENSP00000399168.2:n.*212dup
ENST00000481849.5:n.536dup
ENST00000497377.5:n.700dup
NM_005514.6:c.*212dup	NP_005505.2:n.*212dup
XM_011514556.1:c.*212dup	XP_011512858.1:n.*212dup
XM_011514557.1:c.*212dup	XP_011512859.1:n.*212dup
XR_926175.1:n.1740dup
NM_005514.7:c.*212dup	NP_005505.2:n.*212dup
NM_005514.8:c.*212dup MANE Select	NP_005505.2:n.*212dup