Canonical Allele Identifier: CA1087466547

Gene: HLA-B

Linked Data

• dbSNP Id: rs2113740371
• gnomAD v3: 6-31355902-GTT-G
• gnomAD v4: 6-31355902-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355903_31355904del , CM000668.2:g.31355903_31355904del	GRCh38
NC_000006.11:g.31323680_31323681del , CM000668.1:g.31323680_31323681del	GRCh37
NC_000006.10:g.31431659_31431660del	NCBI36
NG_023187.1:g.6309_6310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2355_2356del
ENST00000481849.6:n.2092+263_2092+264del
ENST00000497377.6:n.2092+263_2092+264del
ENST00000640094.2:c.619+263_619+264del	ENSP00000491275.2:n.619+263_619+264del
ENST00000696558.1:c.620-98_620-97del	ENSP00000512716.1:n.620-98_620-97del
ENST00000696559.1:c.619+263_619+264del	ENSP00000512717.1:n.619+263_619+264del
ENST00000696560.1:c.619+263_619+264del	ENSP00000512718.1:n.619+263_619+264del
ENST00000696561.1:c.619+263_619+264del	ENSP00000512719.1:n.619+263_619+264del
ENST00000696562.1:c.619+263_619+264del	ENSP00000512720.1:n.619+263_619+264del
ENST00000412585.7:c.619+263_619+264del MANE Select	ENSP00000399168.2:n.619+263_619+264del
ENST00000412585.6:c.619+263_619+264del	ENSP00000399168.2:n.619+263_619+264del
ENST00000434333.1:c.652+263_652+264del	ENSP00000405931.1:n.652+263_652+264del
ENST00000474381.1:n.757_758del
ENST00000498007.1:n.885+263_885+264del
NM_005514.6:c.619+263_619+264del	NP_005505.2:n.619+263_619+264del
XM_011514556.1:c.652+263_652+264del	XP_011512858.1:n.652+263_652+264del
XM_011514557.1:c.619+263_619+264del	XP_011512859.1:n.619+263_619+264del
XR_926175.1:n.892_893del
NM_005514.7:c.619+263_619+264del	NP_005505.2:n.619+263_619+264del
NM_005514.8:c.619+263_619+264del MANE Select	NP_005505.2:n.619+263_619+264del