Canonical Allele Identifier: CA822270572

Gene: CCR6

Linked Data

• dbSNP Id: rs1456238791
• gnomAD v3: 6-167119607-A-G
• gnomAD v4: 6-167119607-A-G
• MyVariant Identifiers: chr6:g.167533095A>G (hg19) ; chr6:g.167119607A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119607A>G , CM000668.2:g.167119607A>G	GRCh38
NC_000006.11:g.167533095A>G , CM000668.1:g.167533095A>G	GRCh37
NC_000006.10:g.167453085A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15327A>G
ENST00000705249.1:c.1066-16431A>G	ENSP00000516101.1:n.1066-16431A>G
ENST00000705250.1:c.844-16431A>G	ENSP00000516102.1:n.844-16431A>G
ENST00000705251.1:c.*713-16431A>G	ENSP00000516103.1:n.*713-16431A>G
ENST00000705252.1:c.*536-16431A>G	ENSP00000516104.1:n.*536-16431A>G
ENST00000705253.1:c.*536-16431A>G	ENSP00000516105.1:n.*536-16431A>G
ENST00000705254.1:c.673-16431A>G	ENSP00000516106.1:n.673-16431A>G
ENST00000705255.1:n.1692-16431A>G
ENST00000400926.5:c.-98+7593A>G	ENSP00000383715.2:n.-98+7593A>G
NM_004367.5:c.-98+7593A>G	NP_004358.2:n.-98+7593A>G
XR_943250.1:n.2988T>C
XR_943251.1:n.2988T>C
XR_001744467.2:n.1188-265T>C
XR_001744469.2:n.1118-265T>C
XR_943250.3:n.2755T>C
XR_943251.3:n.2996T>C
NM_004367.6:c.-98+7593A>G	NP_004358.2:n.-98+7593A>G