Canonical Allele Identifier: CA151949739

Gene: CCR6

Linked Data

• dbSNP Id: rs760020891
• gnomAD v2: 6-167533065-AAC-A
• gnomAD v3: 6-167119577-AAC-A
• gnomAD v4: 6-167119577-AAC-A
• MyVariant Identifiers: chr6:g.167533066_167533067del (hg19) ; chr6:g.167119578_167119579del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119581_167119582del , CM000668.2:g.167119581_167119582del	GRCh38
NC_000006.11:g.167533069_167533070del , CM000668.1:g.167533069_167533070del	GRCh37
NC_000006.10:g.167453059_167453060del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15353_2170-15352del
ENST00000705249.1:c.1066-16457_1066-16456del	ENSP00000516101.1:n.1066-16457_1066-16456...
ENST00000705250.1:c.844-16457_844-16456del	ENSP00000516102.1:n.844-16457_844-16456de...
ENST00000705251.1:c.*713-16457_*713-16456del	ENSP00000516103.1:n.*713-16457_*713-16456...
ENST00000705252.1:c.*536-16457_*536-16456del	ENSP00000516104.1:n.*536-16457_*536-16456...
ENST00000705253.1:c.*536-16457_*536-16456del	ENSP00000516105.1:n.*536-16457_*536-16456...
ENST00000705254.1:c.673-16457_673-16456del	ENSP00000516106.1:n.673-16457_673-16456de...
ENST00000705255.1:n.1692-16457_1692-16456del
ENST00000400926.5:c.-98+7567_-98+7568del	ENSP00000383715.2:n.-98+7567_-98+7568del
NM_004367.5:c.-98+7567_-98+7568del	NP_004358.2:n.-98+7567_-98+7568del
XR_943250.1:n.3016_3017del
XR_943251.1:n.3016_3017del
XR_001744467.2:n.1188-237_1188-236del
XR_001744469.2:n.1118-237_1118-236del
XR_943250.3:n.2783_2784del
XR_943251.3:n.3024_3025del
NM_004367.6:c.-98+7567_-98+7568del	NP_004358.2:n.-98+7567_-98+7568del