Canonical Allele Identifier: CA2677957622

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356713-GCGCAGGTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356720_31356728del , CM000668.2:g.31356720_31356728del	GRCh38
NC_000006.11:g.31324497_31324505del , CM000668.1:g.31324497_31324505del	GRCh37
NC_000006.10:g.31432476_31432484del	NCBI36
NG_023187.1:g.5491_5499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1782_1790del
ENST00000481849.6:n.1782_1790del
ENST00000497377.6:n.1782_1790del
ENST00000640094.2:c.309_317del	ENSP00000491275.2:p.Asn104_Arg106del
ENST00000696558.1:c.309_317del	ENSP00000512716.1:p.Asn104_Arg106del
ENST00000696559.1:c.309_317del	ENSP00000512717.1:p.Asn104_Arg106del
ENST00000696560.1:c.309_317del	ENSP00000512718.1:p.Asn104_Arg106del
ENST00000696561.1:c.309_317del	ENSP00000512719.1:p.Asn104_Arg106del
ENST00000696562.1:c.309_317del	ENSP00000512720.1:p.Asn104_Arg106del
ENST00000412585.7:c.309_317del MANE Select	ENSP00000399168.2:p.Asn104_Arg106del
ENST00000412585.6:c.309_317del	ENSP00000399168.2:p.Asn104_Arg106del
ENST00000434333.1:c.342_350del	ENSP00000405931.1:p.Asn115_Arg117del
ENST00000474381.1:n.184_192del
ENST00000498007.1:n.330_338del
ENST00000603274.1:n.74_82del
NM_005514.6:c.309_317del	NP_005505.2:p.Asn104_Arg106del
XM_011514556.1:c.342_350del	XP_011512858.1:p.Asn115_Arg117del
XM_011514557.1:c.309_317del	XP_011512859.1:p.Asn104_Arg106del
XR_926175.1:n.319_327del
NM_005514.7:c.309_317del	NP_005505.2:p.Asn104_Arg106del
NM_005514.8:c.309_317del MANE Select	NP_005505.2:p.Asn104_Arg106del