Canonical Allele Identifier: CA2677956999

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356444-T-TGGCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356452_31356457dup , CM000668.2:g.31356452_31356457dup	GRCh38
NC_000006.11:g.31324229_31324234dup , CM000668.1:g.31324229_31324234dup	GRCh37
NC_000006.10:g.31432208_31432213dup	NCBI36
NG_023187.1:g.5763_5768dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-8_1817-3dup
ENST00000481849.6:n.1817-8_1817-3dup
ENST00000497377.6:n.1817-8_1817-3dup
ENST00000640094.2:c.344-8_344-3dup	ENSP00000491275.2:n.344-8_344-3dup
ENST00000696558.1:c.344-8_344-3dup	ENSP00000512716.1:n.344-8_344-3dup
ENST00000696559.1:c.344-8_344-3dup	ENSP00000512717.1:n.344-8_344-3dup
ENST00000696560.1:c.344-8_344-3dup	ENSP00000512718.1:n.344-8_344-3dup
ENST00000696561.1:c.344-8_344-3dup	ENSP00000512719.1:n.344-8_344-3dup
ENST00000696562.1:c.344-8_344-3dup	ENSP00000512720.1:n.344-8_344-3dup
ENST00000412585.7:c.344-8_344-3dup MANE Select	ENSP00000399168.2:n.344-8_344-3dup
ENST00000412585.6:c.344-8_344-3dup	ENSP00000399168.2:n.344-8_344-3dup
ENST00000434333.1:c.377-8_377-3dup	ENSP00000405931.1:n.377-8_377-3dup
ENST00000474381.1:n.219-8_219-3dup
ENST00000498007.1:n.602_607dup
NM_005514.6:c.344-8_344-3dup	NP_005505.2:n.344-8_344-3dup
XM_011514556.1:c.377-8_377-3dup	XP_011512858.1:n.377-8_377-3dup
XM_011514557.1:c.344-8_344-3dup	XP_011512859.1:n.344-8_344-3dup
XR_926175.1:n.354-8_354-3dup
NM_005514.7:c.344-8_344-3dup	NP_005505.2:n.344-8_344-3dup
NM_005514.8:c.344-8_344-3dup MANE Select	NP_005505.2:n.344-8_344-3dup