Canonical Allele Identifier: CA2677952691

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31353896-TTTGCTCTCTCAAATTCCAGGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353900_31353921del , CM000668.2:g.31353900_31353921del	GRCh38
NC_000006.11:g.31321677_31321698del , CM000668.1:g.31321677_31321698del	GRCh37
NC_000006.10:g.31429656_31429677del	NCBI36
NG_023187.1:g.8295_8316del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3519_3540del
ENST00000481849.6:n.3479_3500del
ENST00000497377.6:n.3386_3407del
ENST00000696558.1:c.1541_1562del	ENSP00000512716.1:n.1541_1562del
ENST00000696559.1:c.*383_*404del	ENSP00000512717.1:n.*383_*404del
ENST00000696560.1:c.*383_*404del	ENSP00000512718.1:n.*383_*404del
ENST00000696561.1:c.*383_*404del	ENSP00000512719.1:n.*383_*404del
ENST00000696562.1:c.*383_*404del	ENSP00000512720.1:n.*383_*404del
ENST00000412585.7:c.*383_*404del MANE Select	ENSP00000399168.2:n.*383_*404del
ENST00000412585.6:c.*383_*404del	ENSP00000399168.2:n.*383_*404del
ENST00000481849.5:n.707_728del
ENST00000497377.5:n.871_892del
NM_005514.6:c.*383_*404del	NP_005505.2:n.*383_*404del
XM_011514556.1:c.*383_*404del	XP_011512858.1:n.*383_*404del
XM_011514557.1:c.*383_*404del	XP_011512859.1:n.*383_*404del
XR_926175.1:n.1911_1932del
NM_005514.7:c.*383_*404del	NP_005505.2:n.*383_*404del
NM_005514.8:c.*383_*404del MANE Select	NP_005505.2:n.*383_*404del