Canonical Allele Identifier: CA2677956555

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356166-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356167_31356168del , CM000668.2:g.31356167_31356168del	GRCh38
NC_000006.11:g.31323944_31323945del , CM000668.1:g.31323944_31323945del	GRCh37
NC_000006.10:g.31431923_31431924del	NCBI36
NG_023187.1:g.6045_6046del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2091_2092del
ENST00000481849.6:n.2091_2092del
ENST00000497377.6:n.2091_2092del
ENST00000640094.2:c.618_619del	ENSP00000491275.2:p.Asp207ProfsTer13
ENST00000696558.1:c.618_619del	ENSP00000512716.1:p.Asp207SerfsTer17
ENST00000696559.1:c.618_619del	ENSP00000512717.1:p.Asp207ProfsTer13
ENST00000696560.1:c.618_619del	ENSP00000512718.1:p.Asp207ProfsTer13
ENST00000696561.1:c.618_619del	ENSP00000512719.1:p.Asp207ProfsTer13
ENST00000696562.1:c.618_619del	ENSP00000512720.1:p.Asp207ProfsTer13
ENST00000412585.7:c.618_619del MANE Select	ENSP00000399168.2:p.Asp207ProfsTer13
ENST00000412585.6:c.618_619del	ENSP00000399168.2:p.Asp207ProfsTer13
ENST00000434333.1:c.651_652del	ENSP00000405931.1:p.Asp218ProfsTer13
ENST00000474381.1:n.493_494del
ENST00000498007.1:n.884_885del
NM_005514.6:c.618_619del	NP_005505.2:p.Asp207ProfsTer13
XM_011514556.1:c.651_652del	XP_011512858.1:p.Asp218ProfsTer13
XM_011514557.1:c.618_619del	XP_011512859.1:p.Asp207ProfsTer13
XR_926175.1:n.628_629del
NM_005514.7:c.618_619del	NP_005505.2:p.Asp207ProfsTer13
NM_005514.8:c.618_619del MANE Select	NP_005505.2:p.Asp207ProfsTer13