Canonical Allele Identifier: CA2677953278

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354241-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354245dup , CM000668.2:g.31354245dup	GRCh38
NC_000006.11:g.31322022dup , CM000668.1:g.31322022dup	GRCh37
NC_000006.10:g.31430001dup	NCBI36
NG_023187.1:g.7971dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3195dup
ENST00000481849.6:n.3155dup
ENST00000497377.6:n.3062dup
ENST00000696558.1:c.1217dup	ENSP00000512716.1:n.1217dup
ENST00000696559.1:c.*59dup	ENSP00000512717.1:n.*59dup
ENST00000696560.1:c.*59dup	ENSP00000512718.1:n.*59dup
ENST00000696561.1:c.*59dup	ENSP00000512719.1:n.*59dup
ENST00000696562.1:c.*59dup	ENSP00000512720.1:n.*59dup
ENST00000412585.7:c.*59dup MANE Select	ENSP00000399168.2:n.*59dup
ENST00000412585.6:c.*59dup	ENSP00000399168.2:n.*59dup
ENST00000481849.5:n.383dup
ENST00000497377.5:n.547dup
NM_005514.6:c.*59dup	NP_005505.2:n.*59dup
XM_011514556.1:c.*59dup	XP_011512858.1:n.*59dup
XM_011514557.1:c.*59dup	XP_011512859.1:n.*59dup
XR_926175.1:n.1587dup
NM_005514.7:c.*59dup	NP_005505.2:n.*59dup
NM_005514.8:c.*59dup MANE Select	NP_005505.2:n.*59dup