Canonical Allele Identifier: CA2677954124

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354475-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354477_31354478del , CM000668.2:g.31354477_31354478del	GRCh38
NC_000006.11:g.31322254_31322255del , CM000668.1:g.31322254_31322255del	GRCh37
NC_000006.10:g.31430233_31430234del	NCBI36
NG_023187.1:g.7736_7737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+2_3140+3del
ENST00000481849.6:n.3100+2_3100+3del
ENST00000497377.6:n.3007+2_3007+3del
ENST00000696558.1:c.1162+2_1162+3del	ENSP00000512716.1:n.1162+2_1162+3del
ENST00000696559.1:c.*4+2_*4+3del	ENSP00000512717.1:n.*4+2_*4+3del
ENST00000696560.1:c.*4+2_*4+3del	ENSP00000512718.1:n.*4+2_*4+3del
ENST00000696561.1:c.*4+2_*4+3del	ENSP00000512719.1:n.*4+2_*4+3del
ENST00000696562.1:c.*4+2_*4+3del	ENSP00000512720.1:n.*4+2_*4+3del
ENST00000412585.7:c.*4+2_*4+3del MANE Select	ENSP00000399168.2:n.*4+2_*4+3del
ENST00000412585.6:c.*4+2_*4+3del	ENSP00000399168.2:n.*4+2_*4+3del
ENST00000481849.5:n.328+2_328+3del
ENST00000497377.5:n.492+2_492+3del
NM_005514.6:c.*4+2_*4+3del	NP_005505.2:n.*4+2_*4+3del
XM_011514556.1:c.*4+2_*4+3del	XP_011512858.1:n.*4+2_*4+3del
XM_011514557.1:c.*4+2_*4+3del	XP_011512859.1:n.*4+2_*4+3del
XR_926175.1:n.1532+2_1532+3del
NM_005514.7:c.*4+2_*4+3del	NP_005505.2:n.*4+2_*4+3del
NM_005514.8:c.*4+2_*4+3del MANE Select	NP_005505.2:n.*4+2_*4+3del