Canonical Allele Identifier: CA2773962289

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119409C>T , CM000668.2:g.167119409C>T	GRCh38
NC_000006.11:g.167532897C>T , CM000668.1:g.167532897C>T	GRCh37
NC_000006.10:g.167452887C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15525C>T
ENST00000705249.1:c.1066-16629C>T	ENSP00000516101.1:n.1066-16629C>T
ENST00000705250.1:c.844-16629C>T	ENSP00000516102.1:n.844-16629C>T
ENST00000705251.1:c.*713-16629C>T	ENSP00000516103.1:n.*713-16629C>T
ENST00000705252.1:c.*536-16629C>T	ENSP00000516104.1:n.*536-16629C>T
ENST00000705253.1:c.*536-16629C>T	ENSP00000516105.1:n.*536-16629C>T
ENST00000705254.1:c.673-16629C>T	ENSP00000516106.1:n.673-16629C>T
ENST00000705255.1:n.1692-16629C>T
ENST00000400926.5:c.-98+7395C>T	ENSP00000383715.2:n.-98+7395C>T
NM_004367.5:c.-98+7395C>T	NP_004358.2:n.-98+7395C>T
XR_943250.1:n.3186G>A
XR_943251.1:n.3186G>A
XR_001744467.2:n.1188-67G>A
XR_001744469.2:n.1118-67G>A
XR_943250.3:n.2953G>A
XR_943251.3:n.3194G>A
NM_004367.6:c.-98+7395C>T	NP_004358.2:n.-98+7395C>T