Canonical Allele Identifier: CA3711671

Gene: HLA-B

Linked Data

• dbSNP Id: rs759615853
• ExAC: 6:31324266 CCCCGA / C
• gnomAD v4: 6-31356489-CCCCGA-C
• MyVariant Identifiers: chr6:g.31324267_31324271del (hg19) ; chr6:g.31356490_31356494del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356492_31356496del , CM000668.2:g.31356492_31356496del	GRCh38
NC_000006.11:g.31324269_31324273del , CM000668.1:g.31324269_31324273del	GRCh37
NC_000006.10:g.31432248_31432252del	NCBI36
NG_023187.1:g.5719_5723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-52_1817-48del
ENST00000481849.6:n.1817-52_1817-48del
ENST00000497377.6:n.1817-52_1817-48del
ENST00000640094.2:c.344-52_344-48del	ENSP00000491275.2:n.344-52_344-48del
ENST00000696558.1:c.344-52_344-48del	ENSP00000512716.1:n.344-52_344-48del
ENST00000696559.1:c.344-52_344-48del	ENSP00000512717.1:n.344-52_344-48del
ENST00000696560.1:c.344-52_344-48del	ENSP00000512718.1:n.344-52_344-48del
ENST00000696561.1:c.344-52_344-48del	ENSP00000512719.1:n.344-52_344-48del
ENST00000696562.1:c.344-52_344-48del	ENSP00000512720.1:n.344-52_344-48del
ENST00000412585.7:c.344-52_344-48del MANE Select	ENSP00000399168.2:n.344-52_344-48del
ENST00000412585.6:c.344-52_344-48del	ENSP00000399168.2:n.344-52_344-48del
ENST00000434333.1:c.377-52_377-48del	ENSP00000405931.1:n.377-52_377-48del
ENST00000474381.1:n.219-52_219-48del
ENST00000498007.1:n.558_562del
NM_005514.6:c.344-52_344-48del	NP_005505.2:n.344-52_344-48del
XM_011514556.1:c.377-52_377-48del	XP_011512858.1:n.377-52_377-48del
XM_011514557.1:c.344-52_344-48del	XP_011512859.1:n.344-52_344-48del
XR_926175.1:n.354-52_354-48del
NM_005514.7:c.344-52_344-48del	NP_005505.2:n.344-52_344-48del
NM_005514.8:c.344-52_344-48del MANE Select	NP_005505.2:n.344-52_344-48del