Canonical Allele Identifier: CA1087460568

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31354449-CCCA-C
• gnomAD v4: 6-31354449-CCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354452_31354454del , CM000668.2:g.31354452_31354454del	GRCh38
NC_000006.11:g.31322229_31322231del , CM000668.1:g.31322229_31322231del	GRCh37
NC_000006.10:g.31430208_31430210del	NCBI36
NG_023187.1:g.7761_7763del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+27_3140+29del
ENST00000481849.6:n.3100+27_3100+29del
ENST00000497377.6:n.3007+27_3007+29del
ENST00000696558.1:c.1162+27_1162+29del	ENSP00000512716.1:n.1162+27_1162+29del
ENST00000696559.1:c.*4+27_*4+29del	ENSP00000512717.1:n.*4+27_*4+29del
ENST00000696560.1:c.*4+27_*4+29del	ENSP00000512718.1:n.*4+27_*4+29del
ENST00000696561.1:c.*4+27_*4+29del	ENSP00000512719.1:n.*4+27_*4+29del
ENST00000696562.1:c.*4+27_*4+29del	ENSP00000512720.1:n.*4+27_*4+29del
ENST00000412585.7:c.*4+27_*4+29del MANE Select	ENSP00000399168.2:n.*4+27_*4+29del
ENST00000412585.6:c.*4+27_*4+29del	ENSP00000399168.2:n.*4+27_*4+29del
ENST00000481849.5:n.328+27_328+29del
ENST00000497377.5:n.492+27_492+29del
NM_005514.6:c.*4+27_*4+29del	NP_005505.2:n.*4+27_*4+29del
XM_011514556.1:c.*4+27_*4+29del	XP_011512858.1:n.*4+27_*4+29del
XM_011514557.1:c.*4+27_*4+29del	XP_011512859.1:n.*4+27_*4+29del
XR_926175.1:n.1532+27_1532+29del
NM_005514.7:c.*4+27_*4+29del	NP_005505.2:n.*4+27_*4+29del
NM_005514.8:c.*4+27_*4+29del MANE Select	NP_005505.2:n.*4+27_*4+29del