Canonical Allele Identifier: CA2677956609

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356257-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356259_31356260del , CM000668.2:g.31356259_31356260del	GRCh38
NC_000006.11:g.31324036_31324037del , CM000668.1:g.31324036_31324037del	GRCh37
NC_000006.10:g.31432015_31432016del	NCBI36
NG_023187.1:g.5954_5955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2000_2001del
ENST00000481849.6:n.2000_2001del
ENST00000497377.6:n.2000_2001del
ENST00000640094.2:c.527_528del	ENSP00000491275.2:p.Glu176GlyfsTer?
ENST00000696558.1:c.527_528del	ENSP00000512716.1:p.Glu176GlyfsTer?
ENST00000696559.1:c.527_528del	ENSP00000512717.1:p.Glu176GlyfsTer?
ENST00000696560.1:c.527_528del	ENSP00000512718.1:p.Glu176GlyfsTer?
ENST00000696561.1:c.527_528del	ENSP00000512719.1:p.Glu176GlyfsTer?
ENST00000696562.1:c.527_528del	ENSP00000512720.1:p.Glu176GlyfsTer?
ENST00000412585.7:c.527_528del MANE Select	ENSP00000399168.2:p.Glu176GlyfsTer?
ENST00000412585.6:c.527_528del	ENSP00000399168.2:p.Glu176GlyfsTer?
ENST00000434333.1:c.560_561del	ENSP00000405931.1:p.Glu187GlyfsTer?
ENST00000474381.1:n.402_403del
ENST00000498007.1:n.793_794del
NM_005514.6:c.527_528del	NP_005505.2:p.Glu176GlyfsTer?
XM_011514556.1:c.560_561del	XP_011512858.1:p.Glu187GlyfsTer?
XM_011514557.1:c.527_528del	XP_011512859.1:p.Glu176GlyfsTer?
XR_926175.1:n.537_538del
NM_005514.7:c.527_528del	NP_005505.2:p.Glu176GlyfsTer?
NM_005514.8:c.527_528del MANE Select	NP_005505.2:p.Glu176GlyfsTer?