Canonical Allele Identifier: CA3711688

Gene: HLA-B

Linked Data

• dbSNP Id: rs764908761
• ExAC: 6:31324430 A / AGGG
• gnomAD v2: 6-31324430-A-AGGG
• gnomAD v3: 6-31356653-A-AGGG
• gnomAD v4: 6-31356653-A-AGGG
• COSMIC: COSN1084000 ; COSN15652586
• MyVariant Identifiers: chr6:g.31324430_31324431insGGG (hg19) ; chr6:g.31356653_31356654insGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356654_31356655insGGG , CM000668.2:g.31356654_31356655insGGG	GRCh38
NC_000006.11:g.31324431_31324432insGGG , CM000668.1:g.31324431_31324432insGGG	GRCh37
NC_000006.10:g.31432410_31432411insGGG	NCBI36
NG_023187.1:g.5559_5560insCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1816+34_1816+35insCCC
ENST00000481849.6:n.1816+34_1816+35insCCC
ENST00000497377.6:n.1816+34_1816+35insCCC
ENST00000640094.2:c.343+34_343+35insCCC	ENSP00000491275.2:n.343+34_343+35insCCC
ENST00000696558.1:c.343+34_343+35insCCC	ENSP00000512716.1:n.343+34_343+35insCCC
ENST00000696559.1:c.343+34_343+35insCCC	ENSP00000512717.1:n.343+34_343+35insCCC
ENST00000696560.1:c.343+34_343+35insCCC	ENSP00000512718.1:n.343+34_343+35insCCC
ENST00000696561.1:c.343+34_343+35insCCC	ENSP00000512719.1:n.343+34_343+35insCCC
ENST00000696562.1:c.343+34_343+35insCCC	ENSP00000512720.1:n.343+34_343+35insCCC
ENST00000412585.7:c.343+34_343+35insCCC MANE Select	ENSP00000399168.2:n.343+34_343+35insCCC
ENST00000412585.6:c.343+34_343+35insCCC	ENSP00000399168.2:n.343+34_343+35insCCC
ENST00000434333.1:c.376+34_376+35insCCC	ENSP00000405931.1:n.376+34_376+35insCCC
ENST00000474381.1:n.218+34_218+35insCCC
ENST00000498007.1:n.398_399insCCC
ENST00000603274.1:n.8_9insGGG
NM_005514.6:c.343+34_343+35insCCC	NP_005505.2:n.343+34_343+35insCCC
XM_011514556.1:c.376+34_376+35insCCC	XP_011512858.1:n.376+34_376+35insCCC
XM_011514557.1:c.343+34_343+35insCCC	XP_011512859.1:n.343+34_343+35insCCC
XR_926175.1:n.353+34_353+35insCCC
NM_005514.7:c.343+34_343+35insCCC	NP_005505.2:n.343+34_343+35insCCC
NM_005514.8:c.343+34_343+35insCCC MANE Select	NP_005505.2:n.343+34_343+35insCCC