Canonical Allele Identifier: CA2773961830

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112658C>G , CM000668.2:g.167112658C>G	GRCh38
NC_000006.11:g.167526146C>G , CM000668.1:g.167526146C>G	GRCh37
NC_000006.10:g.167446136C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22276C>G
ENST00000705249.1:c.1066-23380C>G	ENSP00000516101.1:n.1066-23380C>G
ENST00000705250.1:c.844-23380C>G	ENSP00000516102.1:n.844-23380C>G
ENST00000705251.1:c.*713-23380C>G	ENSP00000516103.1:n.*713-23380C>G
ENST00000705252.1:c.*536-23380C>G	ENSP00000516104.1:n.*536-23380C>G
ENST00000705253.1:c.*536-23380C>G	ENSP00000516105.1:n.*536-23380C>G
ENST00000705254.1:c.673-23380C>G	ENSP00000516106.1:n.673-23380C>G
ENST00000705255.1:n.1692-23380C>G
ENST00000400926.5:c.-98+644C>G	ENSP00000383715.2:n.-98+644C>G
NM_004367.5:c.-98+644C>G	NP_004358.2:n.-98+644C>G
XR_943250.1:n.7839G>C
XR_943251.1:n.7258G>C
XR_001744467.2:n.5774G>C
XR_001744469.2:n.5704G>C
XR_943250.3:n.7606G>C
XR_943251.3:n.7266G>C
NM_004367.6:c.-98+644C>G	NP_004358.2:n.-98+644C>G