Canonical Allele Identifier: CA1680243781

Gene: CCR6

Linked Data

• dbSNP Id: rs1781430433

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112492T>G , CM000668.2:g.167112492T>G	GRCh38
NC_000006.11:g.167525980T>G , CM000668.1:g.167525980T>G	GRCh37
NC_000006.10:g.167445970T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22442T>G
ENST00000705249.1:c.1066-23546T>G	ENSP00000516101.1:n.1066-23546T>G
ENST00000705250.1:c.844-23546T>G	ENSP00000516102.1:n.844-23546T>G
ENST00000705251.1:c.*713-23546T>G	ENSP00000516103.1:n.*713-23546T>G
ENST00000705252.1:c.*536-23546T>G	ENSP00000516104.1:n.*536-23546T>G
ENST00000705253.1:c.*536-23546T>G	ENSP00000516105.1:n.*536-23546T>G
ENST00000705254.1:c.673-23546T>G	ENSP00000516106.1:n.673-23546T>G
ENST00000705255.1:n.1692-23546T>G
ENST00000400926.5:c.-98+478T>G	ENSP00000383715.2:n.-98+478T>G
NM_004367.5:c.-98+478T>G	NP_004358.2:n.-98+478T>G
XR_943250.1:n.8005A>C
XR_943251.1:n.7424A>C
XR_001744467.2:n.5940A>C
XR_001744469.2:n.5870A>C
XR_943250.3:n.7772A>C
XR_943251.3:n.7432A>C
NM_004367.6:c.-98+478T>G	NP_004358.2:n.-98+478T>G