Canonical Allele Identifier: CA136831082

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31321681_31321682insC (hg19) ; chr6:g.31353904_31353905insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353904dup , CM000668.2:g.31353904dup	GRCh38
NC_000006.11:g.31321681dup , CM000668.1:g.31321681dup	GRCh37
NC_000006.10:g.31429660dup	NCBI36
NG_023187.1:g.8309dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3533dup
ENST00000481849.6:n.3493dup
ENST00000497377.6:n.3400dup
ENST00000696558.1:c.1555dup	ENSP00000512716.1:n.1555dup
ENST00000696559.1:c.*397dup	ENSP00000512717.1:n.*397dup
ENST00000696560.1:c.*397dup	ENSP00000512718.1:n.*397dup
ENST00000696561.1:c.*397dup	ENSP00000512719.1:n.*397dup
ENST00000696562.1:c.*397dup	ENSP00000512720.1:n.*397dup
ENST00000412585.7:c.*397dup MANE Select	ENSP00000399168.2:n.*397dup
ENST00000412585.6:c.*397dup	ENSP00000399168.2:n.*397dup
ENST00000481849.5:n.721dup
ENST00000497377.5:n.885dup
NM_005514.6:c.*397dup	NP_005505.2:n.*397dup
XM_011514556.1:c.*397dup	XP_011512858.1:n.*397dup
XM_011514557.1:c.*397dup	XP_011512859.1:n.*397dup
XR_926175.1:n.1925dup
NM_005514.7:c.*397dup	NP_005505.2:n.*397dup
NM_005514.8:c.*397dup MANE Select	NP_005505.2:n.*397dup