Canonical Allele Identifier: CA2713639176

Gene: CCR6

Linked Data

• dbSNP Id: rs2114914023

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119596T>G , CM000668.2:g.167119596T>G	GRCh38
NC_000006.11:g.167533084T>G , CM000668.1:g.167533084T>G	GRCh37
NC_000006.10:g.167453074T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15338T>G
ENST00000705249.1:c.1066-16442T>G	ENSP00000516101.1:n.1066-16442T>G
ENST00000705250.1:c.844-16442T>G	ENSP00000516102.1:n.844-16442T>G
ENST00000705251.1:c.*713-16442T>G	ENSP00000516103.1:n.*713-16442T>G
ENST00000705252.1:c.*536-16442T>G	ENSP00000516104.1:n.*536-16442T>G
ENST00000705253.1:c.*536-16442T>G	ENSP00000516105.1:n.*536-16442T>G
ENST00000705254.1:c.673-16442T>G	ENSP00000516106.1:n.673-16442T>G
ENST00000705255.1:n.1692-16442T>G
ENST00000400926.5:c.-98+7582T>G	ENSP00000383715.2:n.-98+7582T>G
NM_004367.5:c.-98+7582T>G	NP_004358.2:n.-98+7582T>G
XR_943250.1:n.2999A>C
XR_943251.1:n.2999A>C
XR_001744467.2:n.1188-254A>C
XR_001744469.2:n.1118-254A>C
XR_943250.3:n.2766A>C
XR_943251.3:n.3007A>C
NM_004367.6:c.-98+7582T>G	NP_004358.2:n.-98+7582T>G