Canonical Allele Identifier: CA2677956652

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356281-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356282_31356283del , CM000668.2:g.31356282_31356283del	GRCh38
NC_000006.11:g.31324059_31324060del , CM000668.1:g.31324059_31324060del	GRCh37
NC_000006.10:g.31432038_31432039del	NCBI36
NG_023187.1:g.5930_5931del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1976_1977del
ENST00000481849.6:n.1976_1977del
ENST00000497377.6:n.1976_1977del
ENST00000640094.2:c.503_504del	ENSP00000491275.2:p.Gln168ProfsTer8
ENST00000696558.1:c.503_504del	ENSP00000512716.1:p.Gln168ProfsTer8
ENST00000696559.1:c.503_504del	ENSP00000512717.1:p.Gln168ProfsTer8
ENST00000696560.1:c.503_504del	ENSP00000512718.1:p.Gln168ProfsTer8
ENST00000696561.1:c.503_504del	ENSP00000512719.1:p.Gln168ProfsTer8
ENST00000696562.1:c.503_504del	ENSP00000512720.1:p.Gln168ProfsTer8
ENST00000412585.7:c.503_504del MANE Select	ENSP00000399168.2:p.Gln168ProfsTer8
ENST00000412585.6:c.503_504del	ENSP00000399168.2:p.Gln168ProfsTer8
ENST00000434333.1:c.536_537del	ENSP00000405931.1:p.Gln179ProfsTer8
ENST00000474381.1:n.378_379del
ENST00000498007.1:n.769_770del
NM_005514.6:c.503_504del	NP_005505.2:p.Gln168ProfsTer8
XM_011514556.1:c.536_537del	XP_011512858.1:p.Gln179ProfsTer8
XM_011514557.1:c.503_504del	XP_011512859.1:p.Gln168ProfsTer8
XR_926175.1:n.513_514del
NM_005514.7:c.503_504del	NP_005505.2:p.Gln168ProfsTer8
NM_005514.8:c.503_504del MANE Select	NP_005505.2:p.Gln168ProfsTer8