Canonical Allele Identifier: CA2677957756

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356825-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356826_31356828del , CM000668.2:g.31356826_31356828del	GRCh38
NC_000006.11:g.31324603_31324605del , CM000668.1:g.31324603_31324605del	GRCh37
NC_000006.10:g.31432582_31432584del	NCBI36
NG_023187.1:g.5385_5387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1676_1678del
ENST00000481849.6:n.1676_1678del
ENST00000497377.6:n.1676_1678del
ENST00000640094.2:c.203_205del	ENSP00000491275.2:p.Arg68_Glu69delinsLys
ENST00000696558.1:c.203_205del	ENSP00000512716.1:p.Arg68_Glu69delinsLys
ENST00000696559.1:c.203_205del	ENSP00000512717.1:p.Arg68_Glu69delinsLys
ENST00000696560.1:c.203_205del	ENSP00000512718.1:p.Arg68_Glu69delinsLys
ENST00000696561.1:c.203_205del	ENSP00000512719.1:p.Arg68_Glu69delinsLys
ENST00000696562.1:c.203_205del	ENSP00000512720.1:p.Arg68_Glu69delinsLys
ENST00000412585.7:c.203_205del MANE Select	ENSP00000399168.2:p.Arg68_Glu69delinsLys
ENST00000412585.6:c.203_205del	ENSP00000399168.2:p.Arg68_Glu69delinsLys
ENST00000434333.1:c.236_238del	ENSP00000405931.1:p.Arg79_Glu80delinsLys
ENST00000474381.1:n.78_80del
ENST00000498007.1:n.224_226del
ENST00000603274.1:n.180_182del
NM_005514.6:c.203_205del	NP_005505.2:p.Arg68_Glu69delinsLys
XM_011514556.1:c.236_238del	XP_011512858.1:p.Arg79_Glu80delinsLys
XM_011514557.1:c.203_205del	XP_011512859.1:p.Arg68_Glu69delinsLys
XR_926175.1:n.213_215del
NM_005514.7:c.203_205del	NP_005505.2:p.Arg68_Glu69delinsLys
NM_005514.8:c.203_205del MANE Select	NP_005505.2:p.Arg68_Glu69delinsLys