Canonical Allele Identifier: CA2677956845

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356372-GTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356374_31356376del , CM000668.2:g.31356374_31356376del	GRCh38
NC_000006.11:g.31324151_31324153del , CM000668.1:g.31324151_31324153del	GRCh37
NC_000006.10:g.31432130_31432132del	NCBI36
NG_023187.1:g.5838_5840del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1884_1886del
ENST00000481849.6:n.1884_1886del
ENST00000497377.6:n.1884_1886del
ENST00000640094.2:c.411_413del	ENSP00000491275.2:p.Asp138del
ENST00000696558.1:c.411_413del	ENSP00000512716.1:p.Asp138del
ENST00000696559.1:c.411_413del	ENSP00000512717.1:p.Asp138del
ENST00000696560.1:c.411_413del	ENSP00000512718.1:p.Asp138del
ENST00000696561.1:c.411_413del	ENSP00000512719.1:p.Asp138del
ENST00000696562.1:c.411_413del	ENSP00000512720.1:p.Asp138del
ENST00000412585.7:c.411_413del MANE Select	ENSP00000399168.2:p.Asp138del
ENST00000412585.6:c.411_413del	ENSP00000399168.2:p.Asp138del
ENST00000434333.1:c.444_446del	ENSP00000405931.1:p.Asp149del
ENST00000474381.1:n.286_288del
ENST00000498007.1:n.677_679del
NM_005514.6:c.411_413del	NP_005505.2:p.Asp138del
XM_011514556.1:c.444_446del	XP_011512858.1:p.Asp149del
XM_011514557.1:c.411_413del	XP_011512859.1:p.Asp138del
XR_926175.1:n.421_423del
NM_005514.7:c.411_413del	NP_005505.2:p.Asp138del
NM_005514.8:c.411_413del MANE Select	NP_005505.2:p.Asp138del