Canonical Allele Identifier: CA2677955758

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355862-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355866_31355867del , CM000668.2:g.31355866_31355867del	GRCh38
NC_000006.11:g.31323643_31323644del , CM000668.1:g.31323643_31323644del	GRCh37
NC_000006.10:g.31431622_31431623del	NCBI36
NG_023187.1:g.6349_6350del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2395_2396del
ENST00000481849.6:n.2093-272_2093-271del
ENST00000497377.6:n.2093-272_2093-271del
ENST00000640094.2:c.620-272_620-271del	ENSP00000491275.2:n.620-272_620-271del
ENST00000696558.1:c.620-58_620-57del	ENSP00000512716.1:n.620-58_620-57del
ENST00000696559.1:c.620-272_620-271del	ENSP00000512717.1:n.620-272_620-271del
ENST00000696560.1:c.620-272_620-271del	ENSP00000512718.1:n.620-272_620-271del
ENST00000696561.1:c.620-272_620-271del	ENSP00000512719.1:n.620-272_620-271del
ENST00000696562.1:c.620-272_620-271del	ENSP00000512720.1:n.620-272_620-271del
ENST00000412585.7:c.620-272_620-271del MANE Select	ENSP00000399168.2:n.620-272_620-271del
ENST00000412585.6:c.620-272_620-271del	ENSP00000399168.2:n.620-272_620-271del
ENST00000434333.1:c.653-272_653-271del	ENSP00000405931.1:n.653-272_653-271del
ENST00000474381.1:n.797_798del
ENST00000498007.1:n.886-272_886-271del
NM_005514.6:c.620-272_620-271del	NP_005505.2:n.620-272_620-271del
XM_011514556.1:c.653-272_653-271del	XP_011512858.1:n.653-272_653-271del
XM_011514557.1:c.620-272_620-271del	XP_011512859.1:n.620-272_620-271del
XR_926175.1:n.932_933del
NM_005514.7:c.620-272_620-271del	NP_005505.2:n.620-272_620-271del
NM_005514.8:c.620-272_620-271del MANE Select	NP_005505.2:n.620-272_620-271del