Canonical Allele Identifier: CA2773962295

Gene: CCR6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119637C>T , CM000668.2:g.167119637C>T	GRCh38
NC_000006.11:g.167533125C>T , CM000668.1:g.167533125C>T	GRCh37
NC_000006.10:g.167453115C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15297C>T
ENST00000705249.1:c.1066-16401C>T	ENSP00000516101.1:n.1066-16401C>T
ENST00000705250.1:c.844-16401C>T	ENSP00000516102.1:n.844-16401C>T
ENST00000705251.1:c.*713-16401C>T	ENSP00000516103.1:n.*713-16401C>T
ENST00000705252.1:c.*536-16401C>T	ENSP00000516104.1:n.*536-16401C>T
ENST00000705253.1:c.*536-16401C>T	ENSP00000516105.1:n.*536-16401C>T
ENST00000705254.1:c.673-16401C>T	ENSP00000516106.1:n.673-16401C>T
ENST00000705255.1:n.1692-16401C>T
ENST00000400926.5:c.-98+7623C>T	ENSP00000383715.2:n.-98+7623C>T
NM_004367.5:c.-98+7623C>T	NP_004358.2:n.-98+7623C>T
XR_943250.1:n.2958G>A
XR_943251.1:n.2958G>A
XR_001744467.2:n.1188-295G>A
XR_001744469.2:n.1118-295G>A
XR_943250.3:n.2725G>A
XR_943251.3:n.2966G>A
NM_004367.6:c.-98+7623C>T	NP_004358.2:n.-98+7623C>T