Canonical Allele Identifier: CA2677954936

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355123-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355124del , CM000668.2:g.31355124del	GRCh38
NC_000006.11:g.31322901del , CM000668.1:g.31322901del	GRCh37
NC_000006.10:g.31430880del	NCBI36
NG_023187.1:g.7089del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3042del
ENST00000481849.6:n.2561del
ENST00000497377.6:n.2468del
ENST00000640094.2:c.895+193del	ENSP00000491275.2:n.895+193del
ENST00000696558.1:c.1064del	ENSP00000512716.1:n.1064del
ENST00000696559.1:c.995del	ENSP00000512717.1:p.Cys332LeufsTer?
ENST00000696560.1:c.995del	ENSP00000512718.1:p.Cys332LeufsTer?
ENST00000696561.1:c.995del	ENSP00000512719.1:p.Cys332LeufsTer?
ENST00000696562.1:c.995del	ENSP00000512720.1:p.Cys332LeufsTer?
ENST00000412585.7:c.995del MANE Select	ENSP00000399168.2:p.Cys332LeufsTer?
ENST00000640094.1:c.88+193del	ENSP00000491275.1:n.88+193del
ENST00000412585.6:c.995del	ENSP00000399168.2:p.Cys332LeufsTer?
ENST00000463574.1:n.586del
NM_005514.6:c.995del	NP_005505.2:p.Cys332LeufsTer?
XM_011514556.1:c.1028del	XP_011512858.1:p.Cys343LeufsTer?
XM_011514557.1:c.895+193del	XP_011512859.1:n.895+193del
XR_926175.1:n.1434del
NM_005514.7:c.995del	NP_005505.2:p.Cys332LeufsTer?
NM_005514.8:c.995del MANE Select	NP_005505.2:p.Cys332LeufsTer?