Canonical Allele Identifier: CA2677956115

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355996-TTGTCTAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355997_31356003del , CM000668.2:g.31355997_31356003del	GRCh38
NC_000006.11:g.31323774_31323780del , CM000668.1:g.31323774_31323780del	GRCh37
NC_000006.10:g.31431753_31431759del	NCBI36
NG_023187.1:g.6210_6216del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2256_2262del
ENST00000481849.6:n.2092+164_2092+170del
ENST00000497377.6:n.2092+164_2092+170del
ENST00000640094.2:c.619+164_619+170del	ENSP00000491275.2:n.619+164_619+170del
ENST00000696558.1:c.619+164_619+170del	ENSP00000512716.1:n.619+164_619+170del
ENST00000696559.1:c.619+164_619+170del	ENSP00000512717.1:n.619+164_619+170del
ENST00000696560.1:c.619+164_619+170del	ENSP00000512718.1:n.619+164_619+170del
ENST00000696561.1:c.619+164_619+170del	ENSP00000512719.1:n.619+164_619+170del
ENST00000696562.1:c.619+164_619+170del	ENSP00000512720.1:n.619+164_619+170del
ENST00000412585.7:c.619+164_619+170del MANE Select	ENSP00000399168.2:n.619+164_619+170del
ENST00000412585.6:c.619+164_619+170del	ENSP00000399168.2:n.619+164_619+170del
ENST00000434333.1:c.652+164_652+170del	ENSP00000405931.1:n.652+164_652+170del
ENST00000474381.1:n.658_664del
ENST00000498007.1:n.885+164_885+170del
NM_005514.6:c.619+164_619+170del	NP_005505.2:n.619+164_619+170del
XM_011514556.1:c.652+164_652+170del	XP_011512858.1:n.652+164_652+170del
XM_011514557.1:c.619+164_619+170del	XP_011512859.1:n.619+164_619+170del
XR_926175.1:n.793_799del
NM_005514.7:c.619+164_619+170del	NP_005505.2:n.619+164_619+170del
NM_005514.8:c.619+164_619+170del MANE Select	NP_005505.2:n.619+164_619+170del