Canonical Allele Identifier: CA2840383805

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355130_31355132dup , CM000668.2:g.31355130_31355132dup	GRCh38
NC_000006.11:g.31322907_31322909dup , CM000668.1:g.31322907_31322909dup	GRCh37
NC_000006.10:g.31430886_31430888dup	NCBI36
NG_023187.1:g.7081_7083dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3034_3036dup
ENST00000481849.6:n.2553_2555dup
ENST00000497377.6:n.2460_2462dup
ENST00000640094.2:c.895+185_895+187dup	ENSP00000491275.2:n.895+185_895+187dup
ENST00000696558.1:c.1056_1058dup	ENSP00000512716.1:n.1056_1058dup
ENST00000696559.1:c.987_989dup	ENSP00000512717.1:p.Val330_Met331insVal
ENST00000696560.1:c.987_989dup	ENSP00000512718.1:p.Val330_Met331insVal
ENST00000696561.1:c.987_989dup	ENSP00000512719.1:p.Val330_Met331insVal
ENST00000696562.1:c.987_989dup	ENSP00000512720.1:p.Val330_Met331insVal
ENST00000412585.7:c.987_989dup MANE Select	ENSP00000399168.2:p.Val330_Met331insVal
ENST00000640094.1:c.88+185_88+187dup	ENSP00000491275.1:n.88+185_88+187dup
ENST00000412585.6:c.987_989dup	ENSP00000399168.2:p.Val330_Met331insVal
ENST00000463574.1:n.578_580dup
NM_005514.6:c.987_989dup	NP_005505.2:p.Val330_Met331insVal
XM_011514556.1:c.1020_1022dup	XP_011512858.1:p.Val341_Met342insVal
XM_011514557.1:c.895+185_895+187dup	XP_011512859.1:n.895+185_895+187dup
XR_926175.1:n.1426_1428dup
NM_005514.7:c.987_989dup	NP_005505.2:p.Val330_Met331insVal
NM_005514.8:c.987_989dup MANE Select	NP_005505.2:p.Val330_Met331insVal