Canonical Allele Identifier: CA2677954333

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354614-TCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354618_31354621del , CM000668.2:g.31354618_31354621del	GRCh38
NC_000006.11:g.31322395_31322398del , CM000668.1:g.31322395_31322398del	GRCh37
NC_000006.10:g.31430374_31430377del	NCBI36
NG_023187.1:g.7595_7598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+15_3092+18del
ENST00000481849.6:n.3052+15_3052+18del
ENST00000497377.6:n.2959+15_2959+18del
ENST00000640094.2:c.928+15_928+18del	ENSP00000491275.2:n.928+15_928+18del
ENST00000696558.1:c.1114+15_1114+18del	ENSP00000512716.1:n.1114+15_1114+18del
ENST00000696559.1:c.1045+15_1045+18del	ENSP00000512717.1:n.1045+15_1045+18del
ENST00000696560.1:c.1045+15_1045+18del	ENSP00000512718.1:n.1045+15_1045+18del
ENST00000696561.1:c.1045+15_1045+18del	ENSP00000512719.1:n.1045+15_1045+18del
ENST00000696562.1:c.1045+15_1045+18del	ENSP00000512720.1:n.1045+15_1045+18del
ENST00000412585.7:c.1045+15_1045+18del MANE Select	ENSP00000399168.2:n.1045+15_1045+18del
ENST00000640094.1:c.121+15_121+18del	ENSP00000491275.1:n.121+15_121+18del
ENST00000412585.6:c.1045+15_1045+18del	ENSP00000399168.2:n.1045+15_1045+18del
ENST00000481849.5:n.189_192del
ENST00000497377.5:n.444+15_444+18del
NM_005514.6:c.1045+15_1045+18del	NP_005505.2:n.1045+15_1045+18del
XM_011514556.1:c.1078+15_1078+18del	XP_011512858.1:n.1078+15_1078+18del
XM_011514557.1:c.928+15_928+18del	XP_011512859.1:n.928+15_928+18del
XR_926175.1:n.1484+15_1484+18del
NM_005514.7:c.1045+15_1045+18del	NP_005505.2:n.1045+15_1045+18del
NM_005514.8:c.1045+15_1045+18del MANE Select	NP_005505.2:n.1045+15_1045+18del